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Bard® Silicone Uretero-Intestinal Anastomosis Urinary Diversion Stent

FDA UDI

Class II (US FDA UDI)

by C. R. Bard, Inc.

Identity

Trade Name
Bard® Silicone Uretero-Intestinal Anastomosis Urinary Diversion Stent FDA UDI
Generic Name
Polymeric ureteral stent FDA UDI
Device Name
Bard® Silicone Uretero-Intestinal Anastomosis Urinary Diversion Stent with Hydro-Glide™ Guidewire FDA UDI
Model / Reference
089008 FDA UDI
Description
Bard® Silicone Uretero-Intestinal Anastomosis Urinary Diversion Stent with Hydro-Glide™ Guidewire FDA UDI

Identifiers

Catalog Number
089008 FDA UDI
Primary DI / UDI-DI
10801741011655 FDA UDI
FDA Product Code
FAD FDA UDI
GMDN Term
Polymeric ureteral stent FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.4620 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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 90 Centimeter FDA UDI
Catheter Gauge — 8 French FDA UDI

Category: Polymeric ureteral stent

Bard® Silicone Uretero-Intestinal Anastomosis Urinary Diversion Stent by C. R. Bard, Inc. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Polymeric ureteral stent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
C. R. Bard, Inc.

Sources (1)

  • FDA UDI e0f4f297-e5e0-4418-acd0-a54cb6d4a081 36 fields · synced May 30, 2026