← Back to catalogue

GORE VIABIL Biliary Endoprosthesis

FDA UDI

Class II (US FDA UDI)

by W. L. Gore & Associates, Inc

Identity

Trade Name
GORE VIABIL Biliary Endoprosthesis FDA UDI
Generic Name
Polymer-metal biliary stent, non-bioabsorbable FDA UDI
Device Name
VIABIL SHORT WIRE BILIARY ENDO 8mmX6cmX200cm 8.5Fr FDA UDI
Model / Reference
VSWVH0806 FDA UDI
Description
VIABIL SHORT WIRE BILIARY ENDO 8mmX6cmX200cm 8.5Fr FDA UDI

Identifiers

Catalog Number
VSWVH0806 FDA UDI
Primary DI / UDI-DI
00733132638765 FDA UDI
510(k) Number
K170740 FDA UDI
FDA Product Code
FGE FDA UDI
GMDN Term
Polymer-metal biliary stent, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5010 FDA UDI
Commercial Distribution
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
Catheter Gauge — 8.5 French FDA UDI
Outer Diameter — 8 Millimeter FDA UDI
Length — 6 Centimeter FDA UDI

Category: Polymer-metal biliary stent, non-bioabsorbable

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

Similar devices

Also classified as Polymer-metal biliary stent, non-bioabsorbable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI c959d4ab-c2e8-4496-96f7-bd27705f6bd5 37 fields · synced May 29, 2026