No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 00733132638895 | VSWVN0804 | VSWVN0804 | FGE | Catheter, Biliary, Diagnostic | 2 | GORE VIABIL Biliary Endoprosthesis | |
2 | 00733132638888 | VSWVN1010 | VSWVN1010 | FGE | Catheter, Biliary, Diagnostic | 2 | GORE VIABIL Biliary Endoprosthesis | |
3 | 00733132638871 | VSWVN1008 | VSWVN1008 | FGE | Catheter, Biliary, Diagnostic | 2 | GORE VIABIL Biliary Endoprosthesis | |
4 | 00733132638864 | VSWVN1006 | VSWVN1006 | FGE | Catheter, Biliary, Diagnostic | 2 | GORE VIABIL Biliary Endoprosthesis | |
5 | 00733132638857 | VSWVN1004 | VSWVN1004 | FGE | Catheter, Biliary, Diagnostic | 2 | GORE VIABIL Biliary Endoprosthesis | |
6 | 00733132638840 | VSWVN0810 | VSWVN0810 | FGE | Catheter, Biliary, Diagnostic | 2 | GORE VIABIL Biliary Endoprosthesis | |
7 | 00733132638833 | VSWVN0808 | VSWVN0808 | FGE | Catheter, Biliary, Diagnostic | 2 | GORE VIABIL Biliary Endoprosthesis | |
8 | 00733132638826 | VSWVN0806 | VSWVN0806 | FGE | Catheter, Biliary, Diagnostic | 2 | GORE VIABIL Biliary Endoprosthesis | |
9 | 00733132638819 | VSWVH1010 | VSWVH1010 | FGE | Catheter, Biliary, Diagnostic | 2 | GORE VIABIL Biliary Endoprosthesis | |
10 | 00733132638802 | VSWVH1008 | VSWVH1008 | FGE | Catheter, Biliary, Diagnostic | 2 | GORE VIABIL Biliary Endoprosthesis | |
11 | 00733132638796 | VSWVH1006 | VSWVH1006 | FGE | Catheter, Biliary, Diagnostic | 2 | GORE VIABIL Biliary Endoprosthesis | |
12 | 00733132638789 | VSWVH0810 | VSWVH0810 | FGE | Catheter, Biliary, Diagnostic | 2 | GORE VIABIL Biliary Endoprosthesis | |
13 | 00733132638772 | VSWVH0808 | VSWVH0808 | FGE | Catheter, Biliary, Diagnostic | 2 | GORE VIABIL Biliary Endoprosthesis | |
14 | 00733132638765 | VSWVH0806 | VSWVH0806 | FGE | Catheter, Biliary, Diagnostic | 2 | GORE VIABIL Biliary Endoprosthesis | |
15 | 00733132618286 | GEFA017300 | GEFA017300 | 7MM FILTER ON 300CM GUIDEWIRE | NTE | Temporary Carotid Catheter for Embolic Capture | 2 | GORE Embolic Filter |
16 | 00733132618279 | GEFA015185 | GEFA015185 | 5MM FILTER ON 185CM GUIDEWIRE | NTE | Temporary Carotid Catheter for Embolic Capture | 2 | GORE Embolic Filter |
17 | 00733132618262 | GEFA015300 | GEFA015300 | 5MM FILTER ON 300CM GUIDEWIRE | NTE | Temporary Carotid Catheter for Embolic Capture | 2 | GORE Embolic Filter |
18 | 00733132618255 | GEFA017185 | GEFA017185 | 7MM FILTER ON 185CM GUIDEWIRE | NTE | Temporary Carotid Catheter for Embolic Capture | 2 | GORE Embolic Filter |
19 | 00733132617609 | GSXA0015 | GSXA0015 | GORE SEPTAL OCCLUDER 15MM ASD | MLV | Transcatheter Septal Occluder | 3 | Gore Septal Occluder |
20 | 00733132615797 | VN1008200 | VN1008200 | FGE | Catheter, Biliary, Diagnostic | 2 | GORE VIABIL Biliary Endoprosthesis | |
21 | 00733132615773 | VN1008040 | VN1008040 | FGE | Catheter, Biliary, Diagnostic | 2 | GORE VIABIL Biliary Endoprosthesis | |
22 | 00733132615759 | VN1006200 | VN1006200 | FGE | Catheter, Biliary, Diagnostic | 2 | GORE VIABIL Biliary Endoprosthesis | |
23 | 00733132615735 | VN1006040 | VN1006040 | FGE | Catheter, Biliary, Diagnostic | 2 | GORE VIABIL Biliary Endoprosthesis | |
24 | 00733132615711 | VN1004200 | VN1004200 | FGE | Catheter, Biliary, Diagnostic | 2 | GORE VIABIL Biliary Endoprosthesis | |
25 | 00733132615698 | VN1004040 | VN1004040 | FGE | Catheter, Biliary, Diagnostic | 2 | GORE VIABIL Biliary Endoprosthesis | |
26 | 00733132615674 | VN0810200 | VN0810200 | FGE | Catheter, Biliary, Diagnostic | 2 | GORE VIABIL Biliary Endoprosthesis | |
27 | 00733132615650 | VN0810040 | VN0810040 | FGE | Catheter, Biliary, Diagnostic | 2 | GORE VIABIL Biliary Endoprosthesis | |
28 | 00733132615636 | VN0808200 | VN0808200 | FGE | Catheter, Biliary, Diagnostic | 2 | GORE VIABIL Biliary Endoprosthesis | |
29 | 00733132615612 | VN0808040 | VN0808040 | FGE | Catheter, Biliary, Diagnostic | 2 | GORE VIABIL Biliary Endoprosthesis | |
30 | 00733132615599 | VN0806200 | VN0806200 | FGE | Catheter, Biliary, Diagnostic | 2 | GORE VIABIL Biliary Endoprosthesis | |
31 | 00733132615575 | VN0806040 | VN0806040 | FGE | Catheter, Biliary, Diagnostic | 2 | GORE VIABIL Biliary Endoprosthesis | |
32 | 00733132615551 | VN0804200 | VN0804200 | FGE | Catheter, Biliary, Diagnostic | 2 | GORE VIABIL Biliary Endoprosthesis | |
33 | 00733132615537 | VN0804040 | VN0804040 | FGE | Catheter, Biliary, Diagnostic | 2 | GORE VIABIL Biliary Endoprosthesis | |
34 | 00733132615520 | VH1010200 | VH1010200 | FGE | Catheter, Biliary, Diagnostic | 2 | GORE VIABIL Biliary Endoprosthesis | |
35 | 00733132615513 | VH1010040 | VH1010040 | FGE | Catheter, Biliary, Diagnostic | 2 | GORE VIABIL Biliary Endoprosthesis | |
36 | 00733132615506 | VH1008200 | VH1008200 | FGE | Catheter, Biliary, Diagnostic | 2 | GORE VIABIL Biliary Endoprosthesis | |
37 | 00733132615483 | VH1006200 | VH1006200 | FGE | Catheter, Biliary, Diagnostic | 2 | GORE VIABIL Biliary Endoprosthesis | |
38 | 00733132615476 | VH1006040 | VH1006040 | FGE | Catheter, Biliary, Diagnostic | 2 | GORE VIABIL Biliary Endoprosthesis | |
39 | 00733132615469 | VH0810200 | VH0810200 | FGE | Catheter, Biliary, Diagnostic | 2 | GORE VIABIL Biliary Endoprosthesis | |
40 | 00733132615452 | VH0810040 | VH0810040 | FGE | Catheter, Biliary, Diagnostic | 2 | GORE VIABIL Biliary Endoprosthesis | |
41 | 00733132615445 | VH0808200 | VH0808200 | FGE | Catheter, Biliary, Diagnostic | 2 | GORE VIABIL Biliary Endoprosthesis | |
42 | 00733132615438 | VH0808040 | VH0808040 | FGE | Catheter, Biliary, Diagnostic | 2 | GORE VIABIL Biliary Endoprosthesis | |
43 | 00733132615421 | VH0806200 | VH0806200 | FGE | Catheter, Biliary, Diagnostic | 2 | GORE VIABIL Biliary Endoprosthesis | |
44 | 00733132615414 | VH0806040 | VH0806040 | FGE | Catheter, Biliary, Diagnostic | 2 | GORE VIABIL Biliary Endoprosthesis | |
45 | 00733132612154 | SDV2028 | SDV2028 | SDV INTRODUCER SHEATH 20F | DYB | INTRODUCER, CATHETER | 2 | GORE DrySeal Sheath |
46 | 00733132612147 | SDV1828 | SDV1828 | SDV INTRODUCER SHEATH 18F | DYB | INTRODUCER, CATHETER | 2 | GORE DrySeal Sheath |
47 | 00733132612123 | SDV1428 | SDV1428 | SDV INTRODUCER SHEATH 14F | DYB | INTRODUCER, CATHETER | 2 | GORE DrySeal Sheath |
48 | 00733132612116 | SDV1228 | SDV1228 | SDV INTRODUCER SHEATH 12F | DYB | INTRODUCER, CATHETER | 2 | GORE DrySeal Sheath |
49 | 00733132607303 | IRST08080080L | IRST08080080L | INTERING STR T8MM 80CM RS X 80 | DSY | PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER | 2 | GORE INTERING Vascular Graft |
50 | 00733132602001 | 1PDX307 | 1PDX307 | GXQ | Dura Substitute | 2 | GORE PRECLUDE PDX Dura Substitute |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 00878237001325 | M8275080/5 | Vac Abdominal Dressing Featuring Sensatrac Technology | V.A.C.® | KCI USA, INC. | |
2 | 00868047000397 | 31058 | FlexBand 0.7 x 32 Strip | FlexBand | ARTELON | |
3 | 00868047000380 | 31056 | FlexBand 0.7 x 16 Strip | FlexBand | ARTELON | |
4 | 00868047000373 | 31055 | FlexBand 0.7 x 8 Strip | FlexBand | ARTELON | |
5 | 00868047000366 | 31054 | FlexBand 0.5 x 16 Strip | FlexBand | ARTELON | |
6 | 00868047000359 | 31053 | FlexBand 0.5 x 8 Strip | FlexBand | ARTELON | |
7 | 00868047000342 | 31052 | FlexBand 0.3 x 16 Strip | FlexBand | ARTELON | |
8 | 00868047000335 | 31051 | FlexBand 0.3 x 8 Strip | FlexBand | ARTELON | |
9 | 00868047000328 | 31049 | FlexBand 6 x 9 Mesh | FlexBand | ARTELON | |
10 | 00868047000311 | 31050 | FlexBand 3 x 4 Mesh | FlexBand | ARTELON | |
11 | 00868047000304 | 31048 | FlexBand 4 x 6 Mesh | FlexBand | ARTELON | |
12 | 00860000875943 | PTM2025 | DuraSorb Monofilament Mesh | SURGICAL INNOVATION ASSOCIATES, INC. | ||
13 | 00860000875929 | PTM0616 | DuraSorb Monofilament Mesh | SURGICAL INNOVATION ASSOCIATES, INC. | ||
14 | 00860000875905 | PTM1025 | Durasorb Monofilament Mesh | SURGICAL INNOVATION ASSOCIATES, INC. | ||
15 | 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. | |
16 | 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. | |
17 | 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. | |
18 | 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. | |
19 | 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. | |
20 | 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. | |
21 | 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. | |
22 | 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. | |
23 | 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. | |
24 | 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. | |
25 | 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. | |
26 | 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. | |
27 | 00850012832102 | FIHR 40mmE | FIHR 40mmE | The Insightra Medical Freedom Inguinal Hernia Implant (ProFlor™) is a sterile, p The Insightra Medical Freedom Inguinal Hernia Implant (ProFlor™) is a sterile, polypropylene implant device designed for use in the open repair of inguinal hernias. A delivery device, sold separately, is used to deploy the implant into the prepared hernia defect site. | Freedom - ProFlor Inguinal Hernia Implant | INSIGHTRA MEDICAL, INC. |
28 | 00850012832072 | FIHR 40mm | FIHR 40mm | The Insightra Medical Freedom Inguinal Hernia Implant (ProFlor™) is a sterile, p The Insightra Medical Freedom Inguinal Hernia Implant (ProFlor™) is a sterile, polypropylene implant device designed for use in the open repair of inguinal hernias. A delivery device, sold separately, is used to deploy the implant into the prepared hernia defect site. | Freedom - ProFlor Inguinal Hernia Implant | INSIGHTRA MEDICAL, INC. |
29 | 00850012832041 | FIHR 25mmE | FIHR 25mmE | The Insightra Medical Freedom Inguinal Hernia Implant (ProFlor™) is a sterile, p The Insightra Medical Freedom Inguinal Hernia Implant (ProFlor™) is a sterile, polypropylene implant device designed for use in the open repair of inguinal hernias. A delivery device, sold separately, is used to deploy the implant into the prepared hernia defect site. | Freedom - ProFlor Inguinal Hernia Implant | INSIGHTRA MEDICAL, INC. |
30 | 00850012832010 | FIHR 25mm | FIHR 25mm | The Insightra Medical Freedom Inguinal Hernia Implant (ProFlor™) is a sterile, p The Insightra Medical Freedom Inguinal Hernia Implant (ProFlor™) is a sterile, polypropylene implant device designed for use in the open repair of inguinal hernias. A delivery device, sold separately, is used to deploy the implant into the prepared hernia defect site. | Freedom - ProFlor Inguinal Hernia Implant | INSIGHTRA MEDICAL, INC. |
31 | 00850011929247 | T1418-8XD | SurgiMesh | BG MEDICAL, LLC | ||
32 | 00850011929230 | T1116-8XD | SurgiMesh | BG MEDICAL, LLC | ||
33 | 00850011929223 | T1115-8 | SurgiMesh | BG MEDICAL, LLC | ||
34 | 00850011929216 | TEL613-8 | SurgiMesh | BG MEDICAL, LLC | ||
35 | 00850011929209 | T613-8S | SurgiMesh | BG MEDICAL, LLC | ||
36 | 00850011929193 | TEALFIL-8 | SurgiMesh | BG MEDICAL, LLC | ||
37 | 00850011929186 | T3030 | SurgiMesh | BG MEDICAL, LLC | ||
38 | 00850011929179 | T221510 | SurgiMesh | BG MEDICAL, LLC | ||
39 | 00850011929155 | T1415 | SurgiMesh | BG MEDICAL, LLC | ||
40 | 00850011929148 | T1015 | SurgiMesh | BG MEDICAL, LLC | ||
41 | 00850011929131 | T510 | SurgiMesh | BG MEDICAL, LLC | ||
42 | 00850011929124 | Tintra OK-1522 | SurgiMesh | BG MEDICAL, LLC | ||
43 | 00850011929117 | Tintra OK-1015 | SurgiMesh | BG MEDICAL, LLC | ||
44 | 00850011929100 | Tintra CK-10 | SurgiMesh | BG MEDICAL, LLC | ||
45 | 00850011929094 | Tintra CK-7 | SurgiMesh | BG MEDICAL, LLC | ||
46 | 00850011929070 | Tintra O-2636 | SurgiMesh | BG MEDICAL, LLC | ||
47 | 00850011929063 | Tintra E-3030 | SurgiMesh | BG MEDICAL, LLC | ||
48 | 00850011929056 | Tintra E-2226 | SurgiMesh | BG MEDICAL, LLC | ||
49 | 00850011929049 | Tintra E-1522 | SurgiMesh | BG MEDICAL, LLC | ||
50 | 00850011929032 | Tintra R-1415 | SurgiMesh | BG MEDICAL, LLC |