Other products from "TECRES SPA"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 28031497001702 ASC0020 MENDEC AQUA is a sterile single-use device for extrusion into the bone of acryli MENDEC AQUA is a sterile single-use device for extrusion into the bone of acrylic resins or bone void fillers (not supplied with the kit) intended for vertebral augmentation procedures (vertebroplasty, kyphoplasty, screw-augmentation). OAR Injector, Vertebroplasty (Does Not Contain Cement) 1 MENDEC AQUA
2 28031497001429 ASA0380 Shakit is intended for mixing acrylic resins or bone void fillers components. JDZ Mixer, Cement, For Clinical Use 1 Shakit
3 28031497000132 1310/S Cemex System 60g is a polymethylmethacrylate bone cement. Cemex System 60g holds Cemex System 60g is a polymethylmethacrylate bone cement. Cemex System 60g holds the powder (60g) and liquid (22g) components separately within a closed syringe-like device that serves as both a mixing chamber and a cement delivery system.The device is supplied sterile, for single use.Cemex System 60g is indicated for the fixation of joint prosthesis implants to the host bone. LOD Bone Cement 2 CEMEX SYSTEM 60G
4 08031497002897 SPK90Z2 InterSpace Knee ATS Trial Kit is intended to be used for the selection of the ri InterSpace Knee ATS Trial Kit is intended to be used for the selection of the right size and thickness of the InterSpace Knee ATS to be implanted. HWT Template 1 InterSpace Knee ATS Trial Kit
5 08031497002347 SPK90Z1 InterSpace Knee Trial is intended to be used for the selection of the right size InterSpace Knee Trial is intended to be used for the selection of the right size of InterSpace Knee to be implanted. HWT Template 1 InterSpace Knee Trial
6 08031497002101 110043026 Conflow G Bone Cement is a low viscosity antibiotic-loaded polymethylmethacrylat Conflow G Bone Cement is a low viscosity antibiotic-loaded polymethylmethacrylate bone cements. It is composed by two components (40g powder and 14,7g liquid) which are designed for mixing together at the point of use to form the cement. The device is supplied sterile, for single use. Conflow G Bone Cement is indicated for the fixation of prostheses to living bone in the second stage of a two-stage revision for total joint arthroplasty after the initial infection has been cleared. LOD,MBB Bone Cement,Bone Cement, Antibiotic 2 Conflow G Bone Cement
7 08031497001470 ASB0010 BONE INJECTION NEEDLE beveled tip 11 Gauge 120 mm length with plastic handgrip i BONE INJECTION NEEDLE beveled tip 11 Gauge 120 mm length with plastic handgrip intended for the injection of acrylic resin. KIH Dispenser, Cement 1 BONE INJECTION NEEDLE beveled tip 11 Gauge 120 mm length
8 08031497001456 ASC0000 The device is an accessory intended to fill up to six needles or fillers with ac The device is an accessory intended to fill up to six needles or fillers with acrylic resins for vertebroplasty/kyphoplasty at the same time. HXK Holder, Needle; Orthopedic 1 Mendec V FILL
9 08031497000770 ASB0090 BONE INJECTION NEEDLE beveled tip 11 Gauge 120 mm length with metal handgrip int BONE INJECTION NEEDLE beveled tip 11 Gauge 120 mm length with metal handgrip intended for the injection of acrylic resin. KIH Dispenser, Cement 1 BONE INJECTION NEEDLE beveled tip 11 Gauge 120 mm length
10 28031497001870 SPK0422 Temporary Augmented Tibial Stem Spacer with gentamicin. Interspace Knee ATS is c Temporary Augmented Tibial Stem Spacer with gentamicin. Interspace Knee ATS is composed of fully formed gentamicin/polymethylmethacrylate (PMMA), radio-opaque bone cement. The device is sterile and single-use.InterSpace Knee ATS is indicated for temporary use (maximum 180 days) as an adjunct to total knee replacement (TKR) in skeletally mature patients undergoing a two-stage procedure due to a septic process, and where a large tibial defect is present.InterSpace Knee ATS is applied on the tibial plate following removal of the existing implant and radical debridement. The device must be combined with the tibial component of InterSpace Knee. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection).InterSpace Knee ATS is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g. resection arthroplasty, fusion etc.). Because of the inherent mechanical limitations of the device material (gentamicin/ polymethylmethacrylate), the Interspace Knee ATS is only indicated for patients who will consistently use traditional mobility assist devices (e.g. crutches, walkers, canes) throughout the implantation period. JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Interspace Knee ATS 60/07
11 08031497002903 SPK03Z1 InterSpace Knee Trial XL is intended to be used for the selection of the right s InterSpace Knee Trial XL is intended to be used for the selection of the right size of InterSpace Knee XL to be implanted. HWT Template 1 InterSpace Knee Trial XL
12 28031497000071 1220/I Cemex Isoplastic 1/2 pack is a high viscosity polymethylmethacrylate bone cement Cemex Isoplastic 1/2 pack is a high viscosity polymethylmethacrylate bone cement. It is composed by two components (20g powder and 6.65g liquid) which are designed for mixing together at the point of use to form the cement. The device is supplied sterile, for single use.Cemex Isoplastic 1/2 pack is indicated for the fixation of joint prosthesis implants to the host bone. LOD Bone Cement 2 CEMEX ISOPLASTIC 1/2 PACK
13 08031497002330 71271610 RALLY ALL IN ONE CEMENT GUN is intended to be used for helping the extrusion (an RALLY ALL IN ONE CEMENT GUN is intended to be used for helping the extrusion (and hence the delivery) of the bone cement prepared with the RALLY ALL IN ONE SYSTEM devices. KIH Dispenser, Cement 1 RALLY All In One Cement Gun
14 08031497001999 ASB0050 Freezer ring is an accessory intended to be applied to the syringe of Mendec Spi Freezer ring is an accessory intended to be applied to the syringe of Mendec Spine Kit. It allows a longer extrusion time of the resin. KDD Kit, Surgical Instrument, Disposable 1 Freezer Ring
15 08031497000800 ASB0120 BONE INJECTION NEEDLE beveled tip 15 Gauge 120 mm length with plastic handgrip i BONE INJECTION NEEDLE beveled tip 15 Gauge 120 mm length with plastic handgrip intended for the injection of acrylic resin. KIH Dispenser, Cement 1 BONE INJECTION NEEDLE beveled tip 15 Gauge 120 mm length
16 08031497000794 ASB0110 BONE INJECTION NEEDLE beveled tip 15 Gauge 120 mm length with metal handgrip int BONE INJECTION NEEDLE beveled tip 15 Gauge 120 mm length with metal handgrip intended for the injection of acrylic resin. KIH Dispenser, Cement 1 BONE INJECTION NEEDLE beveled tip 15 Gauge 120 mm length
17 08031497000725 SPN1512 BONE INJECTION NEEDLE diamond tip 15 Gauge 120 mm length with plastic handgrip i BONE INJECTION NEEDLE diamond tip 15 Gauge 120 mm length with plastic handgrip intended for the injection of acrylic resin. KIH Dispenser, Cement 1 BONE INJECTION NEEDLE diamond tip 15 Gauge 120 mm length
18 28031497000033 1200/I Cemex Isoplastic is a high viscosity polymethylmethacrylate bone cement. It is c Cemex Isoplastic is a high viscosity polymethylmethacrylate bone cement. It is composed by two components (40g powder and 13.3g liquid) which are designed for mixing together at the point of use to form the cement. The device is supplied sterile, for single use.Cemex Isoplastic is indicated for the fixation of joint prosthesis implants to the host bone. LOD Bone Cement 2 CEMEX ISOPLASTIC
19 08031497002668 SPZ-01 FEMORAL BRUSH facilitates the removal of bone chips and tissue from the medullar FEMORAL BRUSH facilitates the removal of bone chips and tissue from the medullary canal. It is intended to be used for helping the surgeons, during the fixation of artificialjoint prosthesis with the acrylic bone cement, in cleaning the femoral canal from debris after the canal has been drilled and before the cement application. GEC Brush, Scrub, Operating-Room 1 FEMORAL BRUSH
20 08031497002095 110043025 Conflow Bone Cement is a low viscosity polymethylmethacrylate bone cement. It is Conflow Bone Cement is a low viscosity polymethylmethacrylate bone cement. It is composed by two components (40g powder and 13,3g liquid) which are designed for mixing together at the point of use to form the cement. The device is supplied sterile, for single use. Conflow Bone Cement is indicated for the fixation of joint prosthesis implants to the host bone. LOD Bone Cement 2 Conflow Bone Cement
21 08031497000718 SPN1312 BONE INJECTION NEEDLE diamond tip 13 Gauge 120 mm length with plastic handgrip i BONE INJECTION NEEDLE diamond tip 13 Gauge 120 mm length with plastic handgrip intended for the injection of acrylic resin. KIH Dispenser, Cement 1 BONE INJECTION NEEDLE diamond tip 13 Gauge 120 mm length
22 28031497001436 ASA0390 XTRUDER is intended for extrusion of acrylic resins or bone void fillers prepare XTRUDER is intended for extrusion of acrylic resins or bone void fillers prepared with Tecres SHAKIT. KIH Dispenser, Cement 1 XTRUDER
23 28031497001900 SPK0722 Temporary Augmented Tibial Stem Spacer with gentamicin. Interspace Knee ATS is c Temporary Augmented Tibial Stem Spacer with gentamicin. Interspace Knee ATS is composed of fully formed gentamicin/polymethylmethacrylate (PMMA), radio-opaque bone cement. The device is sterile and single-use.InterSpace Knee ATS is indicated for temporary use (maximum 180 days) as an adjunct to total knee replacement (TKR) in skeletally mature patients undergoing a two-stage procedure due to a septic process, and where a large tibial defect is present.InterSpace Knee ATS is applied on the tibial plate following removal of the existing implant and radical debridement. The device must be combined with the tibial component of InterSpace Knee. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection).InterSpace Knee ATS is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g. resection arthroplasty, fusion etc.). Because of the inherent mechanical limitations of the device material (gentamicin/ polymethylmethacrylate), the Interspace Knee ATS is only indicated for patients who will consistently use traditional mobility assist devices (e.g. crutches, walkers, canes) throughout the implantation period. JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Interspace Knee ATS 80/12
24 28031497001382 13C2040 Mendec Spine HV System is indicated for the treatment of pathological fractures Mendec Spine HV System is indicated for the treatment of pathological fractures of the vertebral body using a vertebroplasty or kyphoplasty procedure.Mendec Spine HV System is a closed sysyem which containes the powder and liquid components separately.The device is disposable and sterile. LOD,NDN Bone Cement,Cement, Bone, Vertebroplasty 2 Mendec Spine HV System
25 28031497000514 1500/SG US Cemex Genta System 80g is an antibiotic-loaded polymethylmethacrylate bone cemen Cemex Genta System 80g is an antibiotic-loaded polymethylmethacrylate bone cement. Cemex Genta System 80g holds the powder (80g) and liquid (29,3g) components separately within a closed syringe-like device that serves as both a mixing chamber and a cement delivery system. The device is supplied sterile, for single use.Cemex Genta System 80g is indicated for the fixation of prostheses to living bone in the second stage of a two-stage revision for total joint arthroplasty after the initial infection has been cleared. MBB,LOD Bone Cement, Antibiotic,Bone Cement 2 CEMEX GENTA SYSTEM 80G
26 28031497000507 1400/IG US Cemex Genta HV is a high viscosity antibiotic-loaded polymethylmethacrylate bone Cemex Genta HV is a high viscosity antibiotic-loaded polymethylmethacrylate bone cement. It is composed by two components (40g powder and 14,7g liquid) which are designed for mixing together at the point of use to form the cement. The device is supplied sterile, for single use.Cemex Genta HV is indicated for the fixation of prostheses to living bone in the second stage of a two-stage revision for total joint arthroplasty after the initial infection has been cleared. LOD,MBB Bone Cement,Bone Cement, Antibiotic 2 Cemex Genta HV
27 28031497000354 1510/S Cemex System Fast 70g is a polymethylmethacrylate bone cement with a fast settin Cemex System Fast 70g is a polymethylmethacrylate bone cement with a fast setting. Cemex System Fast 70g holds the powder (70g) and liquid (29,3g) components separately within a closed syringe-like device that serves as both a mixing chamber and a cement delivery system.The device is supplied sterile, for single use.Cemex System Fast 70g is indicated for the fixation of joint prosthesis implants to the host bone. LOD Bone Cement 2 CEMEX SYSTEM FAST 70G
28 28031497000057 1200/S Cemex XL is a low viscosity polymethylmethacrylate bone cement. It is composed b Cemex XL is a low viscosity polymethylmethacrylate bone cement. It is composed by two components (50g powder and 18.33g liquid) which are designed for mixing together at the point of use to form the cement. The device is supplied sterile, for single use.Cemex XL is indicated for the fixation of joint prosthesis implants to the host bone. LOD Bone Cement 2 CEMEX XL
29 08031497002866 SPC90Z3 InterSpace Tapered Wedge Stem Trial is intended to be used for the selection of InterSpace Tapered Wedge Stem Trial is intended to be used for the selection of the right size of InterSpace Tapered Wedge Stem to be implanted. HWT Template 1 InterSpace Tapered Wedge Stem Trial
30 08031497002224 ASA0050 Revision Cannula is intended to be used to distal femoral bone cement delivery t Revision Cannula is intended to be used to distal femoral bone cement delivery through Tecres' Cemex System. KDD Kit, Surgical Instrument, Disposable 1 Revision Cannula
31 08031497002163 65.01.111US MectaCem-X HV with Gentamicin is a low viscosity antibiotic-loaded polymethylme MectaCem-X HV with Gentamicin is a low viscosity antibiotic-loaded polymethylmethacrylate bone cements. It is composed by two components (40g powder and 14,7g liquid) which are designed for mixing together at the point of use to form the cement. The device is supplied sterile, for single use. MectaCem-X HV with Gentamicin is indicated for the fixation of prostheses to living bone in the second stage of a two-stage revision for total joint arthroplasty after the initial infection has been cleared. LOD,MBB Bone Cement,Bone Cement, Antibiotic 2 MectaCem-X HV with Gentamicin
32 08031497000763 ASB0080 BONE INJECTION NEEDLE beveled tip 9 Gauge 150 mm length with metal handgrip inte BONE INJECTION NEEDLE beveled tip 9 Gauge 150 mm length with metal handgrip intended for the injection of acrylic resin. KIH Dispenser, Cement 1 BONE INJECTION NEEDLE beveled tip 9 Gauge 150 mm length
33 08031497000732 ASB0000 BONE INJECTION NEEDLE beveled tip 9 Gauge 150 mm length with plastic handgrip in BONE INJECTION NEEDLE beveled tip 9 Gauge 150 mm length with plastic handgrip intended for the injection of acrylic resin. KIH Dispenser, Cement 1 BONE INJECTION NEEDLE beveled tip 9 Gauge 150 mm length
34 28031497002006 ASC0030 Mendec Aqua Cartridge is intended to be used with Mendec Aqua in vertebral augme Mendec Aqua Cartridge is intended to be used with Mendec Aqua in vertebral augmentation procedure (vertebroplasty, kyphoplasty and screw-augmentation) when the acrylic resin/bone void filler loaded in a single cartridge is not sufficient to complete the surgical procedure. OAR Injector, Vertebroplasty (Does Not Contain Cement) 1 MENDEC AQUA CARTRIDGE
35 28031497000668 SPC0522 Temporary hip spacer with gentamicin. InterSpace Hip is composed of fully formed Temporary hip spacer with gentamicin. InterSpace Hip is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cement coated onto a stainless steel reinforcing structure. The device is sterile and single-use. InterSpace Hip is indicated for temporary use (maximum of 180 days) as a total hip replacement (THR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. The device is inserted into the femoral medullary canal and acetabular cavity following removal of the existing implant and radical debridement. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection). InterSpace Hip is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g., resection arthroplasty, fusion, etc.). MBB,KWL,KWY Bone Cement, Antibiotic,Prosthesis, Hip, Hemi-, Femoral, Metal,Prosthesis, Hip, Bone Cement, Antibiotic,Prosthesis, Hip, Hemi-, Femoral, Metal,Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented 2 InterSpace Hip
36 28031497000958 13A2111 US Cemex Genta System Fast 40g is an antibiotic-loaded polymethylmethacrylate bone Cemex Genta System Fast 40g is an antibiotic-loaded polymethylmethacrylate bone cement. Cemex Genta System Fast 40g holds the powder (40g) and liquid (16,7g) components separately within a closed syringe-like device that serves as both a mixing chamber and a cement delivery system and has a fast setting. The device is supplied sterile, for single use.Cemex Genta System Fast 40g is indicated for the fixation of prostheses to living bone in the second stage of a two-stage revision for total joint arthroplasty after the initial infection has been cleared. MBB,LOD Bone Cement, Antibiotic,Bone Cement 2 CEMEX GENTA SYSTEM FAST 40G
37 28031497000644 SPC0322 Temporary hip spacer with gentamicin. InterSpace Hip is composed of fully formed Temporary hip spacer with gentamicin. InterSpace Hip is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cement coated onto a stainless steel reinforcing structure. The device is sterile and single-use. InterSpace Hip is indicated for temporary use (maximum of 180 days) as a total hip replacement (THR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. The device is inserted into the femoral medullary canal and acetabular cavity following removal of the existing implant and radical debridement. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection). InterSpace Hip is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g., resection arthroplasty, fusion, etc.). MBB,KWL,KWY Bone Cement, Antibiotic,Prosthesis, Hip, Hemi-, Femoral, Metal,Prosthesis, Hip, Bone Cement, Antibiotic,Prosthesis, Hip, Hemi-, Femoral, Metal,Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented 2 InterSpace Hip
38 28031497000521 13C2000 Mendec Spine Kit is a device for the treatment of pathological fractures of the Mendec Spine Kit is a device for the treatment of pathological fractures of the vertebral body using a vertebroplasty procedure.The device is composed by an acrylic resin and a delivery system. NDN Cement, Bone, Vertebroplasty 2 Mendec Spine Kit
39 28031497000637 SPC0222 Temporary hip spacer with gentamicin. InterSpace Hip is composed of fully formed Temporary hip spacer with gentamicin. InterSpace Hip is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cement coated onto a stainless steel reinforcing structure. The device is sterile and single-use. InterSpace Hip is indicated for temporary use (maximum of 180 days) as a total hip replacement (THR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. The device is inserted into the femoral medullary canal and acetabular cavity following removal of the existing implant and radical debridement. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection). InterSpace Hip is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g., resection arthroplasty, fusion, etc.). MBB,KWL,KWY Bone Cement, Antibiotic,Prosthesis, Hip, Hemi-, Femoral, Metal,Prosthesis, Hip, Bone Cement, Antibiotic,Prosthesis, Hip, Hemi-, Femoral, Metal,Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented 2 InterSpace Hip
40 28031497000620 SPC0122 Temporary hip spacer with gentamicin. InterSpace Hip is composed of fully formed Temporary hip spacer with gentamicin. InterSpace Hip is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cement coated onto a stainless steel reinforcing structure. The device is sterile and single-use. InterSpace Hip is indicated for temporary use (maximum of 180 days) as a total hip replacement (THR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. The device is inserted into the femoral medullary canal and acetabular cavity following removal of the existing implant and radical debridement. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection). InterSpace Hip is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g., resection arthroplasty, fusion, etc.). MBB,KWL,KWY Bone Cement, Antibiotic,Prosthesis, Hip, Hemi-, Femoral, Metal,Prosthesis, Hip, Bone Cement, Antibiotic,Prosthesis, Hip, Hemi-, Femoral, Metal,Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented 2 InterSpace Hip
41 28031497000613 SPC0022 Temporary hip spacer with gentamicin. InterSpace Hip is composed of fully formed Temporary hip spacer with gentamicin. InterSpace Hip is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cementcoated onto a stainless steel reinforcing structure. The device is sterile and single-use.InterSpace Hip is indicated for temporary use (maximum of 180 days) as a total hip replacement (THR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. The device is inserted into the femoral medullary canal and acetabular cavity following removal of the existing implant and radical debridement. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection). InterSpace Hip is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g., resection arthroplasty, fusion, etc.). MBB,KWL,KWY Bone Cement, Antibiotic,Prosthesis, Hip, Hemi-, Femoral, Metal,Prosthesis, Hip, Bone Cement, Antibiotic,Prosthesis, Hip, Hemi-, Femoral, Metal,Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented 2 InterSpace Hip
42 28031497000484 1310/SG US Cemex Genta System 60g is an antibiotic-loaded polymethylmethacrylate bone cemen Cemex Genta System 60g is an antibiotic-loaded polymethylmethacrylate bone cement. Cemex Genta System 60g holds the powder (60g) and liquid (22g) components separately within a closed syringe-like device that serves as both a mixing chamber and a cement delivery system. The device is supplied sterile, for single use. Cemex Genta System 60g is indicated for the fixation of prostheses to living bone in the second stage of a two-stage revision for total joint arthroplasty after the initial infection has been cleared. MBB,LOD Bone Cement, Antibiotic,Bone Cement 2 CEMEX GENTA SYSTEM 60G
43 28031497000323 KIT-01 Cemex Prep kit is intended to be used for helping the surgeons during the fixati Cemex Prep kit is intended to be used for helping the surgeons during the fixation of artificial joint prostheses with the acrylic bone cement. The device contains a number of accessories useful during a prosthesis implantation surgery performed using the cementing technique. The components are packaged all together in a unique sterile package single-use. JDK Prosthesis, Hip, Cement Restrictor 2 Cemex Prep Kit
44 08031497002149 65.01.113US MectaCem-X LV with Gentamicin is a low viscosity antibiotic-loaded polymethylmet MectaCem-X LV with Gentamicin is a low viscosity antibiotic-loaded polymethylmethacrylate bone cements. It is composed by two components (40g powder and 14,7g liquid) which are designed for mixing together at the point of use to form the cement. The device is supplied sterile, for single use. MectaCem-X LV with Gentamicin is indicated for the fixation of prostheses to living bone in the second stage of a two-stage revision for total joint arthroplasty after the initial infection has been cleared. LOD,MBB Bone Cement,Bone Cement, Antibiotic 2 MectaCem-X LV with Gentamicin
45 08031497001562 TPA-8 Cement Restrictor designed to be inserted into the femoral medullary canal to li Cement Restrictor designed to be inserted into the femoral medullary canal to limit the flow of bone cement and to aid the cement pressurization during primary or revision hip arthroplasty surgery. It is a single-use and permanent, implantable, sterile device. JDK Prosthesis, Hip, Cement Restrictor 2 Cement Restrictor
46 08031497001418 TPA-24 Cement Restrictor designed to be inserted into the femoral medullary canal to li Cement Restrictor designed to be inserted into the femoral medullary canal to limit the flow of bone cement and to aid the cement pressurization during primary or revision hip arthroplasty surgery. It is a single-use and permanent, implantable, sterile device.Cement Restrictor is provided with the related inserter. JDK Prosthesis, Hip, Cement Restrictor 2 Cement Restrictor
47 08031497001401 TPA-18 Cement Restrictor designed to be inserted into the femoral medullary canal to li Cement Restrictor designed to be inserted into the femoral medullary canal to limit the flow of bone cement and to aid the cement pressurization during primary or revision hip arthroplasty surgery. It is a single-use and permanent, implantable, sterile device. Cement Restrictor is provided with the related inserter. JDK Prosthesis, Hip, Cement Restrictor 2 Cement Restrictor
48 08031497000695 SPN0915 BONE INJECTION NEEDLE diamond tip 9 Gauge 150 mm length with plastic handgrip in BONE INJECTION NEEDLE diamond tip 9 Gauge 150 mm length with plastic handgrip intended for the injection of acrylic resin. KIH Dispenser, Cement 1 BONE INJECTION NEEDLE diamond tip 9 Gauge 150 mm length
49 28031497000217 1500/S Cemex System 80g is a polymethylmethacrylate bone cement. Cemex System 80g holds Cemex System 80g is a polymethylmethacrylate bone cement. Cemex System 80g holds the powder (80g) and liquid (29,3g) components separately within a closed syringe-like device that serves as both a mixing chamber and a cement delivery system.The device is supplied sterile, for single use.Cemex System 80g is indicated for the fixation of joint prosthesis implants to the host bone. LOD Bone Cement 2 CEMEX SYSTEM 80G
50 28031497000538 13A2101 US Cemex Genta System Fast 70g is an antibiotic-loaded polymethylmethacrylate bone Cemex Genta System Fast 70g is an antibiotic-loaded polymethylmethacrylate bone cement. Cemex Genta System Fast 70g holds the powder (70g) and liquid (29,3g) components separately within a closed syringe-like device that serves as both a mixing chamber and a cement delivery system. The device is supplied sterile, for single use. Cemex Genta System Fast 70g is indicated for the fixation of prostheses to living bone in the second stage of a two-stage revision for total joint arthroplasty after the initial infection has been cleared. MBB,LOD Bone Cement, Antibiotic,Bone Cement 2 CEMEX GENTA SYSTEM FAST 70G
Other products with the same Product Codes "MBB, KWL, KWY"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 08806373899546 HA.04B.3604 Head Trial 36XL–offset type BENCOX Hip System CORENTEC CO., LTD
2 08806373899539 HA.04B.3603 Head Trial 36L–offset type BENCOX Hip System CORENTEC CO., LTD
3 08806373899522 HA.04B.3602 Head Trial 36M–offset type BENCOX Hip System CORENTEC CO., LTD
4 08806373899515 HA.04B.3601 Head Trial 36S–offset type BENCOX Hip System CORENTEC CO., LTD
5 08806373899508 HA.04A.3204 Head Trial 32XL–offset type BENCOX Hip System CORENTEC CO., LTD
6 08806373899492 HA.04A.3203 Head Trial 32L–offset type BENCOX Hip System CORENTEC CO., LTD
7 08806373899485 HA.04A.3202 Head Trial 32M–offset type BENCOX Hip System CORENTEC CO., LTD
8 08806373899478 HA.04A.3201 Head Trial 32S–offset type BENCOX Hip System CORENTEC CO., LTD
9 08806373899461 HA.047.2804 Head Trial 28XL–offset type BENCOX Hip System CORENTEC CO., LTD
10 08806373899454 HA.047.2803 Head Trial 28L–offset type BENCOX Hip System CORENTEC CO., LTD
11 08806373899447 HA.047.2802 Head Trial 28M–offset type BENCOX Hip System CORENTEC CO., LTD
12 08806373898853 HA.082.0001 Stem Impactor - Short Bencox Hip System CORENTEC CO., LTD
13 08806373897399 HA.047.2801 Head Trial 28S–offset type BENCOX Hip System CORENTEC CO., LTD
14 08806373897221 HA.081.0021 Bencox M Stem Rasp No.21.5 BENCOX Hip System CORENTEC CO., LTD
15 08806373897214 HA.081.0020 Bencox M Stem Rasp No.20 BENCOX Hip System CORENTEC CO., LTD
16 08806373897207 HA.081.0018 Bencox M Stem Rasp No.18.5 BENCOX Hip System CORENTEC CO., LTD
17 08806373897191 HA.081.0017 Bencox M Stem Rasp No.17 BENCOX Hip System CORENTEC CO., LTD
18 08806373897184 HA.081.0016 Bencox M Stem Rasp No.16 BENCOX Hip System CORENTEC CO., LTD
19 08806373897177 HA.081.0015 Bencox M Stem Rasp No.15 BENCOX Hip System CORENTEC CO., LTD
20 08806373897160 HA.081.0014 Bencox M Stem Rasp No.14 BENCOX Hip System CORENTEC CO., LTD
21 08806373897153 HA.081.0013 Bencox M Stem Rasp No.13 BENCOX Hip System CORENTEC CO., LTD
22 08806373897146 HA.081.0012 Bencox M Stem Rasp No.12 BENCOX Hip System CORENTEC CO., LTD
23 08806373897139 HA.081.0011 Bencox M Stem Rasp No.11 BENCOX Hip System CORENTEC CO., LTD
24 08806373897122 HA.081.0010 Bencox M Stem Rasp No.10 BENCOX Hip System CORENTEC CO., LTD
25 08806373897115 HA.081.0009 Bencox M Stem Rasp No.9 BENCOX Hip System CORENTEC CO., LTD
26 08806373897108 HA.081.0008 Bencox M Stem Rasp No.8 BENCOX Hip System CORENTEC CO., LTD
27 08806373895494 HA.052.4052 BENCOX PE Liner Trial 40/52-Elevated type BENCOX Hip System CORENTEC CO., LTD
28 08806373895487 HA.052.4048 BENCOX PE Liner Trial 40/48-Elevated type BENCOX Hip System CORENTEC CO., LTD
29 08806373895470 HA.052.3652 BENCOX PE Liner Trial 36/52-Elevated type BENCOX Hip System CORENTEC CO., LTD
30 08806373895463 HA.052.3648 BENCOX PE Liner Trial 36/48-Elevated type BENCOX Hip System CORENTEC CO., LTD
31 08806373895456 HA.052.3644 BENCOX PE Liner Trial 36/44-Elevated type BENCOX Hip System CORENTEC CO., LTD
32 08806373895449 HA.052.3252 BENCOX PE Liner Trial 32/52-Elevated type BENCOX Hip System CORENTEC CO., LTD
33 08806373895432 HA.052.3248 BENCOX PE Liner Trial 32/48-Elevated type BENCOX Hip System CORENTEC CO., LTD
34 08806373895425 HA.052.3244 BENCOX PE Liner Trial 32/44-Elevated type BENCOX Hip System CORENTEC CO., LTD
35 08806373895418 HA.052.2839 BENCOX PE Liner Trial 28/39-Elevated type BENCOX Hip System CORENTEC CO., LTD
36 08806373895401 HA.052.2837 BENCOX PE Liner Trial 28/37-Elevated type BENCOX Hip System CORENTEC CO., LTD
37 08806373892677 01.52.500 Primary Stem Extractor Bencox Hip System CORENTEC CO., LTD
38 08806373892240 01.52.167 PE insert trial 40/52G -Standard type BENCOX Hip System CORENTEC CO., LTD
39 08806373892233 01.52.165 PE insert trial 40/48G -Standard type BENCOX Hip System CORENTEC CO., LTD
40 08806373892226 01.52.163 PE insert trial 40/44G -Standard type BENCOX Hip System CORENTEC CO., LTD
41 08806373892219 01.52.157 PE insert trial 36/52G -Standard type BENCOX Hip System CORENTEC CO., LTD
42 08806373892202 01.52.155 PE insert trial 36/48G -Standard type BENCOX Hip System CORENTEC CO., LTD
43 08806373892196 01.52.153 PE insert trial 36/44G -Standard type BENCOX Hip System CORENTEC CO., LTD
44 08806373892189 01.52.147 PE insert trial 32/52G -Standard type BENCOX Hip System CORENTEC CO., LTD
45 08806373892172 01.52.145 PE insert trial 32/48G -Standard type BENCOX Hip System CORENTEC CO., LTD
46 08806373892165 01.52.143 PE insert trial 32/44G -Standard type BENCOX Hip System CORENTEC CO., LTD
47 08806373892158 01.52.132 PE insert trial 28/39G -Standard type BENCOX Hip System CORENTEC CO., LTD
48 08806373892141 01.52.131 PE insert trial 28/37G -Standard type BENCOX Hip System CORENTEC CO., LTD
49 08806373891595 HA.022.0074 Shell trial 74mm (6window) BENCOX Hip System CORENTEC CO., LTD
50 08806373891588 HA.022.0072 Shell trial 72mm (6window) BENCOX Hip System CORENTEC CO., LTD