No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 10884521180260 | TEC1515 | Hydrophilic 2-Dimensional Mesh,Polyester | FTL | Mesh, surgical, polymeric | 2 | Parietex | |
2 | 10884521180345 | TET1510 | Hydrophilic 3-Dimensional Mesh,Polyester | FTL | Mesh, surgical, polymeric | 2 | Parietex | |
3 | 10884521190696 | 89223 | Collagen Implant | FTM | Mesh, surgical | 2 | Enduragen | |
4 | 10884521165724 | PCO8VP | Composite Ventral Patch;Polyester & Polyglycolic-Lactic Acid Patch with Absorbab Composite Ventral Patch;Polyester & Polyglycolic-Lactic Acid Patch with Absorbable Collagen Film | FTL | Mesh, surgical, polymeric | 2 | Parietex | |
5 | 10884521196070 | 89222 | 89222 | Collagen Implant | FTM | Mesh, surgical | 2 | Enduragen |
6 | 10884521196063 | 89220 | 89220 | Collagen Implant | FTM | Mesh, surgical | 2 | Enduragen |
7 | 10884521190719 | 89225 | 89225 | Collagen Implant | FTM | Mesh, surgical | 2 | Enduragen |
8 | 10884521190702 | 89224 | 89224 | Collagen Implant | FTM | Mesh, surgical | 2 | Enduragen |
9 | 10884521190689 | 89221 | 89221 | Collagen Implant | FTM | Mesh, surgical | 2 | Enduragen |
10 | 10884521180321 | TECT1510AL | Hydrophilic Anatomical Mesh,Left Side, Polyester | FTL | Mesh, surgical, polymeric | 2 | Parietex | |
11 | 10884521180314 | TECR3030 | Hydrophilic 2-Dimensional Mesh,Polyester | FTL | Mesh, surgical, polymeric | 2 | Parietex | |
12 | 10884521180291 | TECR1515 | Hydrophilic 2-Dimensional Mesh,Polyester | FTL | Mesh, surgical, polymeric | 2 | Parietex | |
13 | 10884521514164 | PCO8VP | Composite Ventral Patch, Polyester & Polyglycolic-Lactic Acid Patch with Absorba Composite Ventral Patch, Polyester & Polyglycolic-Lactic Acid Patch with Absorbable Collagen Film | FTL | Mesh, surgical, polymeric | 2 | Parietex | |
14 | 10884521180284 | TECR1510 | Hydrophilic 2-Dimensional Mesh,Polyester | FTL | Mesh, surgical, polymeric | 2 | Parietex | |
15 | 10884521180277 | TEC2020 | Hydrophilic 2-Dimensional Mesh,Polyester | FTL | Mesh, surgical, polymeric | 2 | Parietex | |
16 | 10884521514157 | PCO6VP | Composite Ventral Patch, Polyester & Polyglycolic-Lactic Acid Patch with Absorba Composite Ventral Patch, Polyester & Polyglycolic-Lactic Acid Patch with Absorbable Collagen Film | FTL | Mesh, surgical, polymeric | 2 | Parietex | |
17 | 10884521180253 | TEC1510 | Hydrophilic 2-Dimensional Mesh,Polyester | FTL | Mesh, surgical, polymeric | 2 | Parietex | |
18 | 10884521514140 | PCO4VP | Composite Ventral Patch;Polyester & Polyglycolic-Lactic Acid Patch with Absorbab Composite Ventral Patch;Polyester & Polyglycolic-Lactic Acid Patch with Absorbable Collagen Film | FTL | Mesh, surgical, polymeric | 2 | Parietex | |
19 | 10884521180239 | TECT1612AL | Hydrophilic Anatomical Mesh,Left Side, Polyester | FTL | Mesh, surgical, polymeric | 2 | Parietex | |
20 | 10884521180222 | TECT1510ADPR | Hydrophilic Anatomical Mesh,Right Side, Polyester | FTL | Mesh, surgical, polymeric | 2 | Parietex | |
21 | 10884521180215 | TECT1510ADP2R | Hydrophilic Anatomical Mesh,Right Side, Polyester | FTL | Mesh, surgical, polymeric | 2 | Parietex | |
22 | 10884521180208 | TECT1309AL | Hydrophilic Anatomical Mesh,Left Side, Polyester | FTL | Mesh, surgical, polymeric | 2 | Parietex | |
23 | 10884521179837 | PCO2520X | Optimized Composite Mesh,Polyester with Absorbable Collagen Film | FTL | Mesh, surgical, polymeric | 2 | Parietex | |
24 | 10884521179820 | PCO2520OSX | Optimized Composite Mesh,Skirted Polyester Mesh with Absorbable Collagen Film | FTL | Mesh, surgical, polymeric | 2 | Parietex | |
25 | 10884521179813 | PCO2520FX | Optimized Composite Mesh,Skirted Polyester Mesh with Absorbable Collagen Film | FTL | Mesh, surgical, polymeric | 2 | Parietex | |
26 | 10884521179806 | PCO2015OSX | Optimized Composite Mesh,Skirted Polyester Mesh with Absorbable Collagen Film | FTL | Mesh, surgical, polymeric | 2 | Parietex | |
27 | 10884521179790 | PCO15X | Optimized Composite Mesh,Polyester with Absorbable Collagen Film | FTL | Mesh, surgical, polymeric | 2 | Parietex | |
28 | 20884521176451 | PNP8 | Plug and Patch System,Monofilament Polyester and Polylactic Acid Semi-Resorbable Plug and Patch System,Monofilament Polyester and Polylactic Acid Semi-Resorbable Plug with Monofilament Polyester Patch | FTL | Mesh, surgical, polymeric | 2 | Parietex | |
29 | 20884521176444 | PNP6 | Plug and Patch System,Monofilament Polyester and Polylactic Acid Semi-Resorbable Plug and Patch System,Monofilament Polyester and Polylactic Acid Semi-Resorbable Plug with Monofilament Polyester Patch | FTL | Mesh, surgical, polymeric | 2 | Parietex | |
30 | 20884521176437 | PNP8X3 | Plug and Patch System,Monofilament Polyester and Polylactic Acid Semi-Resorbable Plug and Patch System,Monofilament Polyester and Polylactic Acid Semi-Resorbable Plug with Monofilament Polyester Patch | FTL | Mesh, surgical, polymeric | 2 | Parietex | |
31 | 10884521180369 | TET5050 | Hydrophilic 3-Dimensional Mesh,Polyester | FTL | Mesh, surgical, polymeric | 2 | Parietex | |
32 | 10884521180352 | TET2020 | Hydrophilic 3-Dimensional Mesh,Polyester | FTL | Mesh, surgical, polymeric | 2 | Parietex | |
33 | 20884521176420 | PNP6X3 | Plug and Patch System,Monofilament Polyester and Polylactic Acid Semi-Resorbable Plug and Patch System,Monofilament Polyester and Polylactic Acid Semi-Resorbable Plug with Monofilament Polyester Patch | FTL | Mesh, surgical, polymeric | 2 | Parietex | |
34 | 10884523000573 | CRCRP303 | Collagen Repair Patch | FTM | Mesh, surgical | 2 | Permacol | |
35 | 10884523000566 | CRCRP505 | Collagen Repair Patch | FTM | Mesh, surgical | 2 | Permacol | |
36 | 10884523000245 | P152840 | Surgical Implant | FTM | Mesh, surgical | 2 | Permacol | |
37 | 10884523000238 | P152830 | P152830 | Surgical Implant | FTM | Mesh, surgical | 2 | Permacol |
38 | 10884523000221 | P152050 | Surgical Implant | FTM | Mesh, surgical | 2 | Permacol | |
39 | 10884523000214 | P152040 | Surgical Implant | FTM | Mesh, surgical | 2 | Permacol | |
40 | 10884523000207 | P152030 | Surgical Implant | FTM | Mesh, surgical | 2 | Permacol | |
41 | 10884523000191 | P151828 | Surgical Implant | FTM | Mesh, surgical | 2 | Permacol | |
42 | 10884523000184 | P151520 | Surgical Implant | FTM | Mesh, surgical | 2 | Permacol | |
43 | 10884523000177 | P151020 | Surgical Implant | FTM | Mesh, surgical | 2 | Permacol | |
44 | 10884523000160 | P151015 | Surgical Implant | FTM | Mesh, surgical | 2 | Permacol | |
45 | 10884523000146 | P150510 | Surgical Implant | FTM | Mesh, surgical | 2 | Permacol | |
46 | 10884523000139 | P101828 | Surgical Implant | FTM | Mesh, surgical | 2 | Permacol | |
47 | 10884523000122 | P101520 | Surgical Implant | FTM | Mesh, surgical | 2 | Permacol | |
48 | 10884523000115 | P101015 | Surgical Implant | FTM | Mesh, surgical | 2 | Permacol | |
49 | 10884523000108 | P101010 | Surgical Implant | FTM | Mesh, surgical | 2 | Permacol | |
50 | 10884523000092 | P100510 | Surgical Implant | FTM | Mesh, surgical | 2 | Permacol |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 03700386922053 | EBO101 | EBO101 | CEMENT RESTRICTOR | TORNIER | |
2 | 00889024458963 | 32-5014-56 | 32-5014-056-00 | NA | ZIMMER, INC. | |
3 | 00889024458956 | 32-5014-53 | 32-5014-053-00 | NA | ZIMMER, INC. | |
4 | 00868623000360 | XI-S+ | XI0404-S+ | Colorado Therapeutics Xenograft Implant | COLORADO THERAPEUTICS LLC | |
5 | 00868623000353 | XI-S+ | XI0203-S+ | Colorado Therapeutics Xenograft Implant | COLORADO THERAPEUTICS LLC | |
6 | 00868623000346 | XI-S+ | XI0710-S+ | Colorado Therapeutics Xenograft Implant | COLORADO THERAPEUTICS LLC | |
7 | 00868623000339 | XI-S+ | XI0808-S+ | Colorado Therapeutics Xenograft Implant | COLORADO THERAPEUTICS LLC | |
8 | 00868623000322 | XI-S+ | XI0508-S+ | Colorado Therapeutics Xenograft Implant | COLORADO THERAPEUTICS LLC | |
9 | 00868623000315 | XI-S+ | XI0615-S+ | Colorado Therapeutics Xenograft Implant | COLORADO THERAPEUTICS LLC | |
10 | 00868623000308 | XI-S+ | XI0606-S+ | Colorado Therapeutics Xenograft Implant | COLORADO THERAPEUTICS LLC | |
11 | 00860002305141 | XI-S+ | XI0909C-S+ | Colorado Therapeutics Xenograft Implant | COLORADO THERAPEUTICS LLC | |
12 | 00860002305134 | XI-S+ | XI1014B-S+ | Colorado Therapeutics Xenograft Implant | COLORADO THERAPEUTICS LLC | |
13 | 00860002305127 | XI-S+ | XI1014A-S+ | Colorado Therapeutics Xenograft Implant | COLORADO THERAPEUTICS LLC | |
14 | 00860002305110 | XI-S+ | XI1116B-S+ | Colorado Therapeutics Xenograft Implant | COLORADO THERAPEUTICS LLC | |
15 | 00860002305103 | XI-S+ | XI1116A-S+ | Colorado Therapeutics Xenograft Implant | COLORADO THERAPEUTICS LLC | |
16 | 00859389005119 | CMCV-009-XXL | The CanGaroo® Envelope is intended to securely hold a cardiac implantable electr The CanGaroo® Envelope is intended to securely hold a cardiac implantable electronic device or an implantable neurostimulator to create a stable environment when implanted in the body. The cardiac implantable electronic devices that may be used with the CanGaroo® Envelope include pacemaker pulse generators, defibrillators, or other cardiac implantable electronic devices. The implantable neurostimulator devices that may be used with the CanGaroo® Envelope include vagus nerve stimulators, spinal cordneuromodulators, deep brain stimulators and sacral nerve stimulators. | CanGaroo Envelope | AZIYO BIOLOGICS, INC. | |
17 | 00859389005072 | CMCV-009-XLG | The CanGaroo® Envelope is intended to securely hold a cardiac implantable electr The CanGaroo® Envelope is intended to securely hold a cardiac implantable electronic device or an implantable neurostimulator to create a stable environment when implanted in the body. The cardiac implantable electronic devices that may be used with the CanGaroo® Envelope include pacemaker pulse generators, defibrillators, or other cardiac implantable electronic devices. The implantable neurostimulator devices that may be used with the CanGaroo® Envelope include vagus nerve stimulators, spinal cordneuromodulators, deep brain stimulators and sacral nerve stimulators. | CanGaroo Envelope | AZIYO BIOLOGICS, INC. | |
18 | 00859389005065 | CMCV-009-LRG | The CanGaroo® Envelope is intended to securely hold a cardiac implantable electr The CanGaroo® Envelope is intended to securely hold a cardiac implantable electronic device or an implantable neurostimulator to create a stable environment when implanted in the body. The cardiac implantable electronic devices that may be used with the CanGaroo® Envelope include pacemaker pulse generators, defibrillators, or other cardiac implantable electronic devices. The implantable neurostimulator devices that may be used with the CanGaroo® Envelope include vagus nerve stimulators, spinal cordneuromodulators, deep brain stimulators and sacral nerve stimulators. | CanGaroo Envelope | AZIYO BIOLOGICS, INC. | |
19 | 00859389005034 | CMCV-009-MED | The CanGaroo® Envelope is intended to securely hold a cardiac implantable electr The CanGaroo® Envelope is intended to securely hold a cardiac implantable electronic device or an implantable neurostimulator to create a stable environment when implanted in the body. The cardiac implantable electronic devices that may be used with the CanGaroo® Envelope include pacemaker pulse generators, defibrillators, or other cardiac implantable electronic devices. The implantable neurostimulator devices that may be used with the CanGaroo® Envelope include vagus nerve stimulators, spinal cordneuromodulators, deep brain stimulators and sacral nerve stimulators. | CanGaroo Envelope | AZIYO BIOLOGICS, INC. | |
20 | 00859389005027 | CMCV-009-SML | The CanGaroo® Envelope is intended to securely hold a cardiac implantable electr The CanGaroo® Envelope is intended to securely hold a cardiac implantable electronic device or an implantable neurostimulator to create a stable environment when implanted in the body. The cardiac implantable electronic devices that may be used with the CanGaroo® Envelope include pacemaker pulse generators, defibrillators, or other cardiac implantable electronic devices. The implantable neurostimulator devices that may be used with the CanGaroo® Envelope include vagus nerve stimulators, spinal cordneuromodulators, deep brain stimulators and sacral nerve stimulators. | CanGaroo Envelope | AZIYO BIOLOGICS, INC. | |
21 | 00856072005142 | R20243-1122P | OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. | OviTex® PRS | TELA BIO, INC. | |
22 | 00857072005057 | BLM-100-01-1020 | Biologic Matrix | MIROMESH® | REPRISE BIOMEDICAL, INC. | |
23 | 00857072005040 | BLM-100-01-1016 | Biologic Matrix | MIROMESH® | REPRISE BIOMEDICAL, INC. | |
24 | 00857072005033 | BLM-100-01-0816 | Biologic Matrix | MIROMESH® | REPRISE BIOMEDICAL, INC. | |
25 | 00857072005026 | BLM-100-01-1010 | Biologic Matrix | MiroFlex® | REPRISE BIOMEDICAL, INC. | |
26 | 00857072005019 | BLM-100-01-0808 | Biologic Matrix | MiroFlex® | REPRISE BIOMEDICAL, INC. | |
27 | 00857072005002 | BLM-100-01-0608 | Biologic Matrix | MiroFlex® | REPRISE BIOMEDICAL, INC. | |
28 | 00856072005289 | R20252-1020G | OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. | OviTex® PRS | TELA BIO, INC. | |
29 | 00856072005197 | R20253-1122G | OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. | OviTex® PRS | TELA BIO, INC. | |
30 | 00856072005135 | R20243-1018P | OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. | OviTex® PRS | TELA BIO, INC. | |
31 | 00856072005111 | R20153-2020G | OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. | OviTex® PRS | TELA BIO, INC. | |
32 | 00856072005104 | R20153-1620G | OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. | OviTex® PRS | TELA BIO, INC. | |
33 | 00856072005074 | R20143-2020P | OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. | OviTex® PRS | TELA BIO, INC. | |
34 | 00856072005043 | R20143-0416P | OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. | OviTex® PRS | TELA BIO, INC. | |
35 | 00856072005036 | R20252-1122G | OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. | OviTex® PRS | TELA BIO, INC. | |
36 | 00856072005029 | R20252-0815G | OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. | OviTex® PRS | TELA BIO, INC. | |
37 | 00856072005012 | R20152-2020G | OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. | OviTex® PRS | TELA BIO, INC. | |
38 | 00856072005005 | R20152-1620G | OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. | OviTex® PRS | TELA BIO, INC. | |
39 | 00855638007033 | 3102-2152 | Acellular dermal matrix | ProLayer Xenograft | STELLEN MEDICAL, LLC | |
40 | 00855638007026 | 3102-2147 | Acellular Dermal Matrix | ProLayer Xenograft | STELLEN MEDICAL, LLC | |
41 | 00855638007019 | 3102-2144 | Acellular Dermal Matrix | ProLayer Xenograft | STELLEN MEDICAL, LLC | |
42 | 00855638007002 | 3102-2125 | Acellular Dermal Matrix | ProLayer Xenograft | STELLEN MEDICAL, LLC | |
43 | 00854501006036 | 2999-3 | Rotation Medical Reconstituted Collagen Scaffold - Mini-Open, Large | SMITH & NEPHEW, INC. | ||
44 | 00854501006029 | 2999-2 | Rotation Medical Reconstituted Collagen Scaffold - Mini-Open, Medium | SMITH & NEPHEW, INC. | ||
45 | 00840663106349 | e10P16 | e10P16 | XenoSure Biologic Patch, 10cm x 16cm, eIFU | XenoSure Biologic Patch | LEMAITRE VASCULAR, INC. |
46 | 00840663106332 | e8P14 | e8P14 | XenoSure Biologic Patch, 8cm x 14cm, eIFU | XenoSure Biologic Patch | LEMAITRE VASCULAR, INC. |
47 | 00840663106325 | e4P6 | e4P6 | XenoSure Biologic Patch, 4cm x 6cm, eIFU | XenoSure Biologic Patch | LEMAITRE VASCULAR, INC. |
48 | 00840663106318 | e4P4 | e4P4 | XenoSure Biologic Patch, 4cm x 4cm, eIFU | XenoSure Biologic Patch | LEMAITRE VASCULAR, INC. |
49 | 00840663106301 | e2P9 | e2P9 | XenoSure Biologic Patch, 2cm x 9cm, eIFU | XenoSure Biologic Patch | LEMAITRE VASCULAR, INC. |
50 | 00840663106295 | e0.8P8 | e0.8P8 | XenoSure Biologic Patch, 0.8cm x 8cm, eIFU | XenoSure Biologic Patch | LEMAITRE VASCULAR, INC. |