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GORE VIABAHN Endoprosthesis

FDA UDI

Class III (US FDA UDI)

by W. L. Gore & Associates, Inc

Identity

Trade Name
GORE VIABAHN Endoprosthesis FDA UDI
Generic Name
Peripheral artery endovascular stent-graft, non-medicated FDA UDI
Model / Reference
VBC101502 FDA UDI

Identifiers

Catalog Number
VBC101502 FDA UDI
Primary DI / UDI-DI
00733132614691 FDA UDI
PMA Number
P040037 FDA UDI
P130006 FDA UDI
FDA Product Code
NIP FDA UDI
PFV FDA UDI
GMDN Term
Peripheral artery endovascular stent-graft, non-medicated FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Lumen/Inner Diameter — 10 Millimeter FDA UDI
Length — 15 Centimeter FDA UDI

GORE VIABAHN Endoprosthesis by W. L. Gore & Associates, Inc — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

P040037 also covers:

P130006 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
W. L. Gore & Associates, Inc

Sources (1)

  • FDA UDI 9d54ad23-ff8c-48bf-804a-c574f999e207 37 fields · synced Jun 8, 2026