No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 00386190001295 | PFM1015 | PFM1015 | Pelvic Floor Matrix 10 x 15 cm | FTM,OXH | Mesh, surgical,Mesh, surgical, collagen, plastic and reconstructive surgery | 2 | ACell® |
2 | 00386190001288 | PFM0912 | PFM0912 | Pelvic Floor Matrix 9 x 12 cm | OXH,FTM | Mesh, surgical, collagen, plastic and reconstructive surgery,Mesh, surgical | 2 | ACell® |
3 | 00386190001271 | PFM0710 | PFM0710 | Pelvic Floor Matrix 7 x 10 cm | FTM,OXH | Mesh, surgical,Mesh, surgical, collagen, plastic and reconstructive surgery | 2 | ACell® |
4 | 00386190001264 | PFM0505 | PFM0505 | Pelvic Floor Matrix 5 x 5 cm | OXH,FTM | Mesh, surgical, collagen, plastic and reconstructive surgery,Mesh, surgical | 2 | ACell® |
5 | 00386190001257 | PFM0412 | PFM0412 | Pelvic Floor Matrix 4 x 12 cm | OXH,FTM | Mesh, surgical, collagen, plastic and reconstructive surgery,Mesh, surgical | 2 | ACell® |
6 | 00386190001202 | MM1000 | MM1000 | MicroMatrix, 1000 mg | KGN | DRESSING, WOUND, COLLAGEN | U | MicroMatrix® |
7 | 00386190001196 | MM0200F | MM0200F | MicroMatrix, 200 mg Fine Particulate | KGN | DRESSING, WOUND, COLLAGEN | U | MicroMatrix® |
8 | 00386190001189 | MM0500 | MM0500 | MicroMatrix, 500 mg | KGN | DRESSING, WOUND, COLLAGEN | U | MicroMatrix® |
9 | 00386190001172 | MM0200 | MM0200 | MicroMatrix, 200 mg | KGN | DRESSING, WOUND, COLLAGEN | U | MicroMatrix® |
10 | 00386190001165 | MM0100F | MM0100F | MicroMatrix, 100 mg Fine Particulate | KGN | DRESSING, WOUND, COLLAGEN | U | MicroMatrix® |
11 | 00386190001158 | MM0100 | MM0100 | MicroMatrix, 100 mg | KGN | DRESSING, WOUND, COLLAGEN | U | MicroMatrix® |
12 | 00386190001141 | MM0060 | MM0060 | MicroMatrix, 60 mg | KGN | DRESSING, WOUND, COLLAGEN | U | MicroMatrix® |
13 | 00386190001134 | MM0030 | MM0030 | MicroMatrix, 30 mg | KGN | DRESSING, WOUND, COLLAGEN | U | MicroMatrix® |
14 | 00386190001127 | MM0020 | MM0020 | MicroMatrix, 20 mg | KGN | DRESSING, WOUND, COLLAGEN | U | MicroMatrix® |
15 | 00386190001080 | WS1015 | WS1015 | Wound Matrix 1- Layer 10 x 15 cm | KGN | DRESSING, WOUND, COLLAGEN | U | Cytal® |
16 | 00386190001073 | WS0710 | WS0710 | Wound Matrix 1- Layer 7 x 10 cm | KGN | DRESSING, WOUND, COLLAGEN | U | Cytal® |
17 | 00386190001066 | WS0307 | WS0307 | Wound Matrix 1- Layer 3 x 7 cm | KGN | DRESSING, WOUND, COLLAGEN | U | Cytal® |
18 | 00386190001059 | WS0303 | WS0303 | Wound Matrix 1- Layer 3 x 3.5 cm | KGN | DRESSING, WOUND, COLLAGEN | U | Cytal® |
19 | 00386190001042 | WSM1015 | WSM1015 | Wound Matrix 2-Layer 10 x 15 cm | KGN | DRESSING, WOUND, COLLAGEN | U | Cytal® |
20 | 00386190001035 | WSM0710 | WSM0710 | Wound Matrix 2-Layer 7 x 10 cm | KGN | DRESSING, WOUND, COLLAGEN | U | Cytal® |
21 | 00386190001028 | WSM0505 | WSM0505 | Wound Matrix 2-Layer 5 x 5 cm | KGN | DRESSING, WOUND, COLLAGEN | U | Cytal® |
22 | 00386190000939 | WSR0505 | WSR0505 | Wound Matrix 3-Layer 5 x 5 cm | KGN | DRESSING, WOUND, COLLAGEN | U | Cytal® |
23 | 00386190001837 | WSR1635 | WSR1635 | Wound Matrix 3-Layer 16 x 35 cm | KGN | DRESSING, WOUND, COLLAGEN | U | Cytal® |
24 | 00386190001820 | WSR1625 | WSR1625 | Wound Matrix 3-Layer 16 x 25 cm | KGN | DRESSING, WOUND, COLLAGEN | U | Cytal® |
25 | 00386190001516 | WSX1015 | WSX1015 | Wound Matrix 6-Layer 10 x 15 cm | KGN | DRESSING, WOUND, COLLAGEN | U | Cytal® |
26 | 00386190001509 | WSX0710 | WSX0710 | Wound Matrix 6-Layer 7 x 10 cm | KGN | DRESSING, WOUND, COLLAGEN | U | Cytal® |
27 | 00386190001493 | WSX0505 | WSX0505 | Wound Matrix 6-Layer 5 x 5 cm | KGN | DRESSING, WOUND, COLLAGEN | U | Cytal® |
28 | 00386190001486 | WSR1015 | WSR1015 | Wound Matrix 3-Layer 10 x 15 cm | KGN | DRESSING, WOUND, COLLAGEN | U | Cytal® |
29 | 00386190001479 | WSR0710 | WSR0710 | Wound Matrix 3-Layer 7 x 10 cm | KGN | DRESSING, WOUND, COLLAGEN | U | Cytal® |
30 | 00386190001462 | WSR0505 | WSR0505 | Wound Matrix 3-Layer 5 x 5 cm | KGN | DRESSING, WOUND, COLLAGEN | U | Cytal® |
31 | 00386190001455 | WSM1015 | WSM1015 | Wound Matrix 2-Layer 10 x 15 cm | KGN | DRESSING, WOUND, COLLAGEN | U | Cytal® |
32 | 00386190001448 | WSM0710 | WSM0710 | Wound Matrix 2-Layer 7 x 10 cm | KGN | DRESSING, WOUND, COLLAGEN | U | Cytal® |
33 | 00386190001431 | WSM0505 | WSM0505 | Wound Matrix 2-Layer 5 x 5 cm | KGN | DRESSING, WOUND, COLLAGEN | U | Cytal® |
34 | 00386190001424 | WS1015 | WS1015 | Wound Matrix 1-Layer 10 x 15 cm | KGN | DRESSING, WOUND, COLLAGEN | U | Cytal® |
35 | 00386190001417 | WS0710 | WS0710 | Wound Matrix 1-Layer 7 x 10 cm | KGN | DRESSING, WOUND, COLLAGEN | U | Cytal® |
36 | 00386190001110 | BMM1015 | BMM1015 | Burn Matrix 10 x 15 cm | KGN | DRESSING, WOUND, COLLAGEN | U | Cytal® |
37 | 00386190001103 | BMM0710 | BMM0710 | Burn Matrix 7 x 10 cm | KGN | DRESSING, WOUND, COLLAGEN | U | Cytal® |
38 | 00386190001097 | BMM0505 | BMM0505 | Burn Matrix 5 x 5 cm | KGN | DRESSING, WOUND, COLLAGEN | U | Cytal® |
39 | 00386190001004 | BMM0710 | BMM0710 | Burn Matrix 7 X 10 cm | KGN | DRESSING, WOUND, COLLAGEN | U | Cytal® |
40 | 00386190000991 | BMM1015 | BMM1015 | Burn Matrix 10 X 15 cm | KGN | DRESSING, WOUND, COLLAGEN | U | Cytal® |
41 | 00386190000984 | WSX1015 | WSX1015 | Wound Matrix 6-Layer 10 x 15 cm | KGN | DRESSING, WOUND, COLLAGEN | U | Cytal® |
42 | 00386190000977 | WSX0710 | WSX0710 | Wound Matrix 6-Layer 7 x 10 cm | KGN | DRESSING, WOUND, COLLAGEN | U | Cytal® |
43 | 00386190000960 | WSX0505 | WSX0505 | Wound Matrix 6-Layer 5 x 5 cm | KGN | DRESSING, WOUND, COLLAGEN | U | Cytal® |
44 | 00386190000953 | WSR1015 | WSR1015 | Wound Matrix 3-Layer 10 x 15 cm | KGN | DRESSING, WOUND, COLLAGEN | U | Cytal® |
45 | 00386190000946 | WSR0710 | WSR0710 | Wound Matrix 3-Layer 7 x 10 cm | KGN | DRESSING, WOUND, COLLAGEN | U | Cytal® |
46 | 00386190001011 | BMM0505 | BMM0505 | Burn Matrix 5 X 5 cm | KGN | DRESSING, WOUND, COLLAGEN | U | Cytal® |
47 | 00386190001400 | WS0307 | WS0307 | Wound Matrix 1-Layer 3 x 7 cm | KGN | DRESSING, WOUND, COLLAGEN | U | Cytal® |
48 | 00386190001394 | WS0303 | WS0303 | Wound Matrix 1-Layer 3 x 3.5 cm | KGN | DRESSING, WOUND, COLLAGEN | U | Cytal® |
49 | 00386190002087 | PP1015 | PP1015 | for Pericardial Repair, 10 x 15 cm | PSQ | Intracardiac patch or pledget, biologically derived | 2 | Cardion™ |
50 | 00386190002070 | PP0710 | PP0710 | for Pericardial Repair, 7 x 10 cm | PSQ | Intracardiac patch or pledget, biologically derived | 2 | Cardion™ |
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 | 00868623000360 | XI-S+ | XI0404-S+ | Colorado Therapeutics Xenograft Implant | COLORADO THERAPEUTICS LLC | |
6 | 00868623000353 | XI-S+ | XI0203-S+ | Colorado Therapeutics Xenograft Implant | COLORADO THERAPEUTICS LLC | |
7 | 00868623000353 | XI-S+ | XI0203-S+ | Colorado Therapeutics Xenograft Implant | COLORADO THERAPEUTICS LLC | |
8 | 00868623000346 | XI-S+ | XI0710-S+ | Colorado Therapeutics Xenograft Implant | COLORADO THERAPEUTICS LLC | |
9 | 00868623000346 | XI-S+ | XI0710-S+ | Colorado Therapeutics Xenograft Implant | COLORADO THERAPEUTICS LLC | |
10 | 00868623000339 | XI-S+ | XI0808-S+ | Colorado Therapeutics Xenograft Implant | COLORADO THERAPEUTICS LLC | |
11 | 00868623000339 | XI-S+ | XI0808-S+ | Colorado Therapeutics Xenograft Implant | COLORADO THERAPEUTICS LLC | |
12 | 00868623000322 | XI-S+ | XI0508-S+ | Colorado Therapeutics Xenograft Implant | COLORADO THERAPEUTICS LLC | |
13 | 00868623000322 | XI-S+ | XI0508-S+ | Colorado Therapeutics Xenograft Implant | COLORADO THERAPEUTICS LLC | |
14 | 00868623000315 | XI-S+ | XI0615-S+ | Colorado Therapeutics Xenograft Implant | COLORADO THERAPEUTICS LLC | |
15 | 00868623000315 | XI-S+ | XI0615-S+ | Colorado Therapeutics Xenograft Implant | COLORADO THERAPEUTICS LLC | |
16 | 00868623000308 | XI-S+ | XI0606-S+ | Colorado Therapeutics Xenograft Implant | COLORADO THERAPEUTICS LLC | |
17 | 00868623000308 | XI-S+ | XI0606-S+ | Colorado Therapeutics Xenograft Implant | COLORADO THERAPEUTICS LLC | |
18 | 00860002305141 | XI-S+ | XI0909C-S+ | Colorado Therapeutics Xenograft Implant | COLORADO THERAPEUTICS LLC | |
19 | 00860002305141 | XI-S+ | XI0909C-S+ | Colorado Therapeutics Xenograft Implant | COLORADO THERAPEUTICS LLC | |
20 | 00860002305134 | XI-S+ | XI1014B-S+ | Colorado Therapeutics Xenograft Implant | COLORADO THERAPEUTICS LLC | |
21 | 00860002305134 | XI-S+ | XI1014B-S+ | Colorado Therapeutics Xenograft Implant | COLORADO THERAPEUTICS LLC | |
22 | 00860002305127 | XI-S+ | XI1014A-S+ | Colorado Therapeutics Xenograft Implant | COLORADO THERAPEUTICS LLC | |
23 | 00860002305127 | XI-S+ | XI1014A-S+ | Colorado Therapeutics Xenograft Implant | COLORADO THERAPEUTICS LLC | |
24 | 00860002305110 | XI-S+ | XI1116B-S+ | Colorado Therapeutics Xenograft Implant | COLORADO THERAPEUTICS LLC | |
25 | 00860002305110 | XI-S+ | XI1116B-S+ | Colorado Therapeutics Xenograft Implant | COLORADO THERAPEUTICS LLC | |
26 | 00860002305103 | XI-S+ | XI1116A-S+ | Colorado Therapeutics Xenograft Implant | COLORADO THERAPEUTICS LLC | |
27 | 00860002305103 | XI-S+ | XI1116A-S+ | Colorado Therapeutics Xenograft Implant | COLORADO THERAPEUTICS LLC | |
28 | 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. | |
29 | 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. | |
30 | 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. | |
31 | 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. | |
32 | 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. | |
33 | 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. | |
34 | 00857072005057 | BLM-100-01-1020 | Biologic Matrix | MIROMESH® | REPRISE BIOMEDICAL, INC. | |
35 | 00857072005057 | BLM-100-01-1020 | Biologic Matrix | MIROMESH® | REPRISE BIOMEDICAL, INC. | |
36 | 00857072005040 | BLM-100-01-1016 | Biologic Matrix | MIROMESH® | REPRISE BIOMEDICAL, INC. | |
37 | 00857072005040 | BLM-100-01-1016 | Biologic Matrix | MIROMESH® | REPRISE BIOMEDICAL, INC. | |
38 | 00857072005033 | BLM-100-01-0816 | Biologic Matrix | MIROMESH® | REPRISE BIOMEDICAL, INC. | |
39 | 00857072005033 | BLM-100-01-0816 | Biologic Matrix | MIROMESH® | REPRISE BIOMEDICAL, INC. | |
40 | 00857072005026 | BLM-100-01-1010 | Biologic Matrix | MiroFlex® | REPRISE BIOMEDICAL, INC. | |
41 | 00857072005026 | BLM-100-01-1010 | Biologic Matrix | MiroFlex® | REPRISE BIOMEDICAL, INC. | |
42 | 00857072005019 | BLM-100-01-0808 | Biologic Matrix | MiroFlex® | REPRISE BIOMEDICAL, INC. | |
43 | 00857072005019 | BLM-100-01-0808 | Biologic Matrix | MiroFlex® | REPRISE BIOMEDICAL, INC. | |
44 | 00857072005002 | BLM-100-01-0608 | Biologic Matrix | MiroFlex® | REPRISE BIOMEDICAL, INC. | |
45 | 00857072005002 | BLM-100-01-0608 | Biologic Matrix | MiroFlex® | REPRISE BIOMEDICAL, INC. | |
46 | 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. | |
47 | 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. | |
48 | 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. | |
49 | 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. | |
50 | 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. |