No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 00613994499677 | 8220325 | MUTING PROBE 8220325 NIM | GWF,ETN | STIMULATOR, ELECTRICAL, EVOKED RESPONSE,STIMULATOR, NERVE | 2 | NIM® | |
2 | 00681490030069 | 1028081 | VENT TUBE 1028081 5PK HOFFMAN PERM LINER | ETD | TUBE, TYMPANOSTOMY | 2 | NA | |
3 | 00885074371177 | 1160050 | PROSTHESIS 1160050 TI PART VINCENT HA | ETB,ETA | PROSTHESIS, PARTIAL OSSICULAR REPLACEMENT,REPLACEMENT, OSSICULAR PROSTHESIS, TOTAL | 2 | NA | |
4 | 00885074371160 | 1160000 | PROSTHESIS 1160000 TI PARTIAL RND 2MM | ETB,ETA | PROSTHESIS, PARTIAL OSSICULAR REPLACEMENT,REPLACEMENT, OSSICULAR PROSTHESIS, TOTAL | 2 | NA | |
5 | 00885074525075 | 31312055 | BUR 31312055 2MM STD LENGTH | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
6 | 00885074525068 | 31312554 | BUR 31312554 2.5MM STD LENGTH | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
7 | 00885074525051 | 31311071 | BUR 31311071 1MM LONG LENGTH | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
8 | 00885074525044 | 31311570 | BUR 31311570 1.5MM LONG LENGTH | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
9 | 00885074525037 | 31312070 | BUR 31312070 2MM LONG LENGTH | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
10 | 00885074525020 | 31312569 | BUR 31312569 2.5MM LONG LENGTH | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
11 | 00885074525006 | 31314053UE | BUR 31314053UE ULTRA 4MM STD LENGTH | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
12 | 00885074524955 | 31313069UE | BUR 31313069UE ULTRA 3MM LONG LENGTH | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
13 | 00885074524948 | 31313568UE | BUR 31313568UE ULTRA 3.5MM LONG LENGTH | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
14 | 00885074524931 | 31314068UE | BUR 31314068UE ULTRA 4MM LONG LENGTH | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
15 | 00885074524924 | 31315066UE | BUR 31315066UE ULTRA 5MM LONG LENGTH | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
16 | 00885074524917 | 31316063UE | BUR 31316063UE ULTRA 6MM LONG LENGTH | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
17 | 00885074524900 | 31317062UE | BUR 31317062UE ULTRA 7MM LONG LENGTH | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
18 | 00885074497006 | 31111075 | BUR 31111075 1MMX75MM CRSE DIAMOND | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
19 | 00885074496993 | 31111575 | BUR 31111575 1.5MMX75MM CRSE DIAMOND | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
20 | 00885074496986 | 31112075 | BUR 31112075 2MMX75MM CRSE DIAMOND | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
21 | 00885074496962 | 31112575 | BUR 31112575 2.5MMX75MM CRSE DIAMOND | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
22 | 00885074496948 | 31113075 | BUR 31113075 3MMX75MM CRSE DIAMOND | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
23 | 00885074496924 | 31114075 | BUR 31114075 4MMX75MM CRSE DIAMOND | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
24 | 00885074496900 | 31246064 | BUR 31246064 6MM CRSE DIAMOND PEAR LONG | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
25 | 00885074496856 | 31131056 | BUR 31131056 1MM FINE DIAMOND STD | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
26 | 00885074496849 | 31131555 | BUR 31131555 1.5MM FINE DIAMOND STD | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
27 | 00885074496832 | 31132055 | BUR 31132055 2MM FINE DIAMOND STD | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
28 | 00885074496726 | 31132554 | BUR 31132554 2.5MM FINE DIAMOND STD | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
29 | 00885074496719 | 31133054 | BUR 31133054 3MM FINE DIAMOND STD | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
30 | 00885074496702 | 31133553 | BUR 31133553 3.5MM FINE DIAMOND STD | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
31 | 00885074496696 | 31134053 | BUR 31134053 4MM FINE DIAMOND STD | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
32 | 00885074496658 | 31136050 | BUR 31136050 6MM FINE DIAMOND STD | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
33 | 00885074496641 | 31130571 | BUR 31130571 0.5MM FINE DIAMOND LONG | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
34 | 00885074496634 | 31131071 | BUR 31131071 1MM FINE DIAMOND LONG | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
35 | 00885074496627 | 31131570 | BUR 31131570 1.5MM FINE DIAMOND LONG | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
36 | 00885074496610 | 31132070 | BUR 31132070 2MM FINE DIAMOND LONG | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
37 | 00885074496597 | 31132569 | BUR 31132569 2.5MM FINE DIAMOND LONG | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
38 | 00885074496580 | 31133069 | BUR 31133069 3MM FINE DIAMOND LONG | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
39 | 00885074496573 | 31133568 | BUR 31133568 3.5MM FINE DIAMOND LONG | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
40 | 00885074496566 | 31134068 | BUR 31134068 4MM FINE DIAMOND LONG | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
41 | 00885074496559 | 31135066 | BUR 31135066 5MM FINE DIAMOND LONG | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
42 | 00885074496542 | 31136065 | BUR 31136065 6MM FINE DIAMOND LONG | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
43 | 00885074496535 | 31111056 | BUR 31111056 1MM CRSE DIAMOND STD | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
44 | 00885074496528 | 31111555 | BUR 31111555 1.5MM CRSE DIAMOND STD | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
45 | 00885074496511 | 31112055 | BUR 31112055 2MM CRSE DIAMOND STD | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
46 | 00885074496498 | 31112554 | BUR 31112554 2.5MM CRSE DIAMOND STD | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
47 | 00885074496481 | 31113054 | BUR 31113054 3MM CRSE DIAMOND STD | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
48 | 00885074496467 | 31114053 | BUR 31114053 4MM CRSE DIAMOND STD | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
49 | 00885074496450 | 31116050 | BUR 31116050 6MM CRSE DIAMOND STD | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A | |
50 | 00885074496443 | 31111071 | BUR 31111071 1MM CRSE DIAMOND LONG | EQJ | BUR, EAR, NOSE AND THROAT | 1 | N/A |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | B330OT02240 | OT-0224 | The Osseoflex® SB is designed for use in balloon kyphoplasty. The balloon serves The Osseoflex® SB is designed for use in balloon kyphoplasty. The balloon serves to create a cavity in the vertebral body, thereby reducing the fracture while still allowing for cement interdigitation. The balloon catheter is the functional part of the device that creates a cavity and reduces the fracture. The balloon catheter provides a conduit through which the physician can inflate the balloon at the distal end of the catheter. After the bone is disrupted, PMMA is injected through an Osseoflex® SN steerable needle to fill the previously created void(s).An access channel is required for Osseoflex® SB placement. The Osseoflex® SB device does not create an access channel; the Osseoflex SB is designed to follow a pre-existing channel created by an access channel device. If the balloon has an Articulating Stylet inserted it enables the steerable feature of the balloon. The articulating or steering feature of the device assists the clinician in directing the device through the pre-existing channel. The Osseoflex® SB actuation knob can be turned clockwise to aid in directing the distal portion of the device. Turning the actuation knob counter-clockwise will relax the device and allow the device to be returned to its start position. The device should be manipulated only while under fluoroscopic observation with radiographic equipment that provides high quality images. | Osseoflex SB Straight Balloon (10ga/4ml) | OSSEON LLC | |
2 | B330OT02220 | OT-0222 | The Osseoflex® SB is designed for use in balloon kyphoplasty. The balloon serves The Osseoflex® SB is designed for use in balloon kyphoplasty. The balloon serves to create a cavity in the vertebral body, thereby reducing the fracture while still allowing for cement interdigitation. The balloon catheter is the functional part of the device that creates a cavity and reduces the fracture. The balloon catheter provides a conduit through which the physician can inflate the balloon at the distal end of the catheter. After the bone is disrupted, PMMA is injected through an Osseoflex® SN steerable needle to fill the previously created void(s).An access channel is required for Osseoflex® SB placement. The Osseoflex® SB device does not create an access channel; the Osseoflex® SB is designed to follow a pre-existing channel created by an access channel device. If the balloon has an Articulating Stylet inserted it enables the steerable feature of the balloon. The articulating or steering feature of the device assists the clinician in directing the device through the pre-existing channel. The Osseoflex® SB actuation knob can be turned clockwise to aid in directing the distal portion of the device. Turning the actuation knob counter-clockwise will relax the device and allow the device to be returned to its start position. The device should be manipulated only while under fluoroscopic observation with radiographic equipment that provides high quality images. | Osseoflex SB Straight Balloon (10ga/2ml) | OSSEON LLC | |
3 | B330OF82220 | OF-8222 | The Osseoflex® SB is designed for use in balloon kyphoplasty. The balloon serves The Osseoflex® SB is designed for use in balloon kyphoplasty. The balloon serves to create a cavity in the vertebral body, thereby reducing the fracture while still allowing for cement interdigitation. The balloon catheter is the functional part of the device that creates a cavity and reduces the fracture. The balloon catheter provides a conduit through which the physician can inflate the balloon at the distal end of the catheter. After the bone is disrupted, PMMA is injected through an Osseoflex® SN+ steerable needle to fill the previously created void(s).An access channel is required for Osseoflex® SB placement. The Osseoflex® SB device does not create an access channel; the Osseoflex® SB is designed to follow a pre-existing channel created by an access channel device. The articulating or steering feature of the device assists the clinician in directing the device through the pre-existingchannel. The Osseoflex® SB knob can be turned clockwise to aid in directing the distal portion of the device. Turning the knob counter-clockwise will relax the device and allow the device to be returned to its start position. The device should be manipulated only while under fluoroscopic observation with radiographic equipment that provides high quality images. | Osseoflex SB Steerable Balloon (8ga/2ml) | OSSEON LLC | |
4 | B330OF02240 | OF-0224 | The Osseoflex® SB is designed for use in balloon kyphoplasty. The balloon serves The Osseoflex® SB is designed for use in balloon kyphoplasty. The balloon serves to create a cavity in the vertebral body, thereby reducing the fracture while still allowing for cement interdigitation. The balloon catheter is the functional part of the device that creates a cavity and reduces the fracture. The balloon catheter provides a conduit through which the physician can inflate the balloon at the distal end of the catheter. After the bone is disrupted, PMMA is injected through an Osseoflex® SN steerable needle to fill the previously created void(s).An access channel is required for Osseoflex® SB placement. The Osseoflex® SB device does not create an access channel; the Osseoflex® SB is designed to follow a pre-existing channel created by an access channel device.If the balloon has an Articulating Stylet inserted it enables the steerable feature of the balloon. The articulating or steering feature of the device assists the clinician in directing the device through the pre-existing channel. The Osseoflex® SB actuation knob can be turned clockwise to aid in directing the distal portion of the device. Turning the actuation knob counter-clockwise will relax the device and allow the device to be returned to its start position. The device should be manipulated only while under fluoroscopic observation with radiographic equipment that provides high quality images. | Osseoflex SB Steerable Balloon ( 10 ga/ 4ml) | OSSEON LLC | |
5 | B330OF02220 | OF-0222 | The Osseoflex® SB is designed for use in balloon kyphoplasty. The balloon serves The Osseoflex® SB is designed for use in balloon kyphoplasty. The balloon serves to create a cavity in the vertebral body, thereby reducing the fracture while still while still allowing for cement interdigitation. The balloon catheter is the functional part of the device that creates a cavity and reduces the fracture. The balloon catheter provides a conduit through which the physician can inflate the balloon at the distal end of the catheter. After the bone is disrupted, PMMA is injected through an Osseoflex® SN steerable needle to fill the previously created void(s). An access channel is required for the Osseoflex® SB placement. The Osseoflex® SB device does not create an access channel; the Osseoflex® SB is designed to follow a pre-existing channel created by an access channel device.If the balloon has an Articulating Stylet inserted it enables the steerable feature of the balloon. The articulating or steering feature of the device assists the clinician in directing the device through the pre-existing channel. The Osseoflex® SB actuation knob can be turned clockwise to aid in directing the distal portion of the device. Turning the actuation knob counter-clockwise will relax the device and allow the device to be returned to it's start position. The device should be manipulated only while under fluoroscopic observation with radiographic equipment that provides high quality images. | Osseoflex SB Steerable Balloon (10ga/2ml) | OSSEON LLC | |
6 | B330OF00050 | OF-0005 | The Osseoflex® SB is designed for use in balloon kyphoplasty. The balloon serves The Osseoflex® SB is designed for use in balloon kyphoplasty. The balloon serves to create a cavity in the vertebral body, thereby reducing the fracture while still allowing for cement interdigitation. The balloon catheter is the functional part of the device that creates a cavity and reduces the fracture. The balloon catheter provides a conduit through which the physician can inflate the balloon at the distal end of the catheter. After the bone is disrupted, PMMA is injected through an Osseoflex® SN+ steerable needle to fill the previously created void(s).An access channel is required for Osseoflex® SB placement. The Osseoflex® SB device does not create an access channel; the Osseoflex® SB is designed to follow a pre-existing channel created by an access channel device. The articulating or steering feature of the device assists the clinician in directing the device through the pre-existingchannel. The Osseoflex® SB knob can be turned clockwise to aid in directing the distal portion of the device. Turning the knob counter-clockwise will relax the device and allow the device to be returned to its start position. The device should be manipulated only while under fluoroscopic observation with radiographic equipment that provides high quality images. | Osseoflex SB Steerable Balloon (8ga/ 4ml) | OSSEON LLC | |
7 | B278K0051011E0 | K0051011E | K0051011E | CYLINDRICAL REAMER 11MM | ELEOS™ | ONKOS SURGICAL, INC. |
8 | B278K0051023E0 | K0051023E | K0051023E | CYLINDRICAL REAMER 23MM | ELEOS™ | ONKOS SURGICAL, INC. |
9 | B278K0051022E0 | K0051022E | K0051022E | CYLINDRICAL REAMER 22MM | ELEOS™ | ONKOS SURGICAL, INC. |
10 | B278K0051021E0 | K0051021E | K0051021E | CYLINDRICAL REAMER 21MM | ELEOS™ | ONKOS SURGICAL, INC. |
11 | B278K0051020E0 | K0051020E | K0051020E | CYLINDRICAL REAMER 20MM | ELEOS™ | ONKOS SURGICAL, INC. |
12 | B278K0051019E0 | K0051019E | K0051019E | CYLINDRICAL REAMER 19MM | ELEOS™ | ONKOS SURGICAL, INC. |
13 | B278K0051018E0 | K0051018E | K0051018E | CYLINDRICAL REAMER 18MM | ELEOS™ | ONKOS SURGICAL, INC. |
14 | B278K0051017E0 | K0051017E | K0051017E | CYLINDRICAL REAMER 17MM | ELEOS™ | ONKOS SURGICAL, INC. |
15 | B278K0051016E0 | K0051016E | K0051016E | CYLINDRICAL REAMER 16MM | ELEOS™ | ONKOS SURGICAL, INC. |
16 | B278K0051015E0 | K0051015E | K0051015E | CYLINDRICAL REAMER 15MM | ELEOS™ | ONKOS SURGICAL, INC. |
17 | B278K0051014E0 | K0051014E | K0051014E | CYLINDRICAL REAMER 14MM | ELEOS™ | ONKOS SURGICAL, INC. |
18 | B278K0051013E0 | K0051013E | K0051013E | CYLINDRICAL REAMER 13MM | ELEOS™ | ONKOS SURGICAL, INC. |
19 | B278K0051012E0 | K0051012E | K0051012E | CYLINDRICAL REAMER 12MM | ELEOS™ | ONKOS SURGICAL, INC. |
20 | B278K0051010E0 | K0051010E | K0051010E | CYLINDRICAL REAMER 10MM | ELEOS™ | ONKOS SURGICAL, INC. |
21 | B278K0050522E0 | K0050522E | K0050522E | CYLINDRICAL REAMER 22.5MM | ELEOS™ | ONKOS SURGICAL, INC. |
22 | B278K0050521E0 | K0050521E | K0050521E | CYLINDRICAL REAMER 21.5MM | ELEOS™ | ONKOS SURGICAL, INC. |
23 | B278K0050520E0 | K0050520E | K0050520E | CYLINDRICAL REAMER 20.5MM | ELEOS™ | ONKOS SURGICAL, INC. |
24 | B278K0050519E0 | K0050519E | K0050519E | CYLINDRICAL REAMER 19.5MM | ELEOS™ | ONKOS SURGICAL, INC. |
25 | B278K0050518E0 | K0050518E | K0050518E | CYLINDRICAL REAMER 18.5MM | ELEOS™ | ONKOS SURGICAL, INC. |
26 | B278K0050517E0 | K0050517E | K0050517E | CYLINDRICAL REAMER 17.5MM | ELEOS™ | ONKOS SURGICAL, INC. |
27 | B278K0050516E0 | K0050516E | K0050516E | CYLINDRICAL REAMER 16.5MM | ELEOS™ | ONKOS SURGICAL, INC. |
28 | B278K0050515E0 | K0050515E | K0050515E | CYLINDRICAL REAMER 15.5MM | ELEOS™ | ONKOS SURGICAL, INC. |
29 | B278K0050514E0 | K0050514E | K0050514E | CYLINDRICAL REAMER 14.5MM | ELEOS™ | ONKOS SURGICAL, INC. |
30 | B278K0050513E0 | K0050513E | K0050513E | CYLINDRICAL REAMER 13.5MM | ELEOS™ | ONKOS SURGICAL, INC. |
31 | B278K0050512E0 | K0050512E | K0050512E | CYLINDRICAL REAMER 12.5MM | ELEOS™ | ONKOS SURGICAL, INC. |
32 | B278K0050511E0 | K0050511E | K0050511E | CYLINDRICAL REAMER 11.5MM | ELEOS™ | ONKOS SURGICAL, INC. |
33 | B278K0050510E0 | K0050510E | K0050510E | CYLINDRICAL REAMER 10.5MM | ELEOS™ | ONKOS SURGICAL, INC. |
34 | B278K0031013E0 | K0031013E | K0031013E | RESURFACING PATELLA PEG DRILL | ELEOS™ | ONKOS SURGICAL, INC. |
35 | B27825107614E0 | 25107614E | 25107614E | TIBIAL BASEPLATE CEMENTED REAMER | ELEOS™ | ONKOS SURGICAL, INC. |
36 | B27825107613E0 | 25107613E | 25107613E | TIBIAL BASEPLATE PRESS FIT REAMER | ELEOS™ | ONKOS SURGICAL, INC. |
37 | B27825107211E0 | 25107211E | 25107211E | RESECTION PLANER 11MM | ELEOS™ | ONKOS SURGICAL, INC. |
38 | B27825107209E0 | 25107209E | 25107209E | RESECTION PLANER 9MM | ELEOS™ | ONKOS SURGICAL, INC. |
39 | B27825107207E0 | 25107207E | 25107207E | RESECTION PLANER 7MM | ELEOS™ | ONKOS SURGICAL, INC. |
40 | B27825107201E0 | 25107201E | 25107201E | UNIVERSAL RESECTION PLANER | ELEOS™ | ONKOS SURGICAL, INC. |
41 | B235MDK00010 | MDK-0001 | MDK-0001 | mild Device Kit | VERTOS MEDICAL, INC. | |
42 | B192300311000 | 30-0311-00 | 30-0311-00 | 4.0 mm, 45 deg. Sinuscope, l=175mm, autoclavable | IEC-Innoview GmbH | INNOVATIVE ENDOSCOPY COMPONENTS, L.L.C. |
43 | B192300012000 | 30-0012-00 | 30-0012-00 | 4.0 mm, 70 deg. Arthroscope, l=175mm, autoclavable | IEC-Innoview GmbH | INNOVATIVE ENDOSCOPY COMPONENTS, L.L.C. |
44 | B192300011000 | 30-0011-00 | 30-0011-00 | 4.0 mm, 30 deg. Arthroscope, l=175mm, autoclavable | IEC-Innoview GmbH | INNOVATIVE ENDOSCOPY COMPONENTS, L.L.C. |
45 | B192300010000 | 30-0010-00 | 30-0010-00 | 4.0 mm, 0 deg. Arthroscope, l=175mm, autoclavable | IEC-Innoview GmbH | INNOVATIVE ENDOSCOPY COMPONENTS, L.L.C. |
46 | B192300008000 | 30-0008-00 | 30-0008-00 | 2.7 mm, 30 deg. Arthroscope, l=187.5mm, autoclavable | IEC-Innoview GmbH | INNOVATIVE ENDOSCOPY COMPONENTS, L.L.C. |
47 | B192300006000 | 30-0006-00 | 30-0006-00 | 2.7 mm, 70 deg. Arthroscope, l=175mm, autoclavable | IEC-Innoview GmbH | INNOVATIVE ENDOSCOPY COMPONENTS, L.L.C. |
48 | B192300004000 | 30-0004-00 | 30-0004-00 | 2.7 mm, 0 deg. Arthroscope, l=175mm, autoclavable | IEC-Innoview GmbH | INNOVATIVE ENDOSCOPY COMPONENTS, L.L.C. |
49 | B192300003000 | 30-0003-00 | 30-0003-00 | 2.7 mm, 70 deg. Arthroscope, l=110mm, autoclavable | IEC-Innoview GmbH | INNOVATIVE ENDOSCOPY COMPONENTS, L.L.C. |
50 | B089B659660 | B65966 | B65966 | ENDOPLASTIC SCOPE; 12''(33CM, )30 DEGREE, 10MM DIAMETER, | ENDOPLASTIC SCOPE | BLACK & BLACK SURGICAL, INC. |