← Back to catalogue

Bard Wire-Guided Jejunal Feeding/Gastric Decompression Tube

FDA UDI

Class II (US FDA UDI)

by Bard Access Systems, Inc.

Identity

Trade Name
Bard Wire-Guided Jejunal Feeding/Gastric Decompression Tube FDA UDI
Generic Name
Gastrojejunostomy tube FDA UDI
Device Name
Bard Wire-Guided Jejunal Feeding/Gastric Decompression Tube 12F FDA UDI
Model / Reference
000734 FDA UDI
Description
Bard Wire-Guided Jejunal Feeding/Gastric Decompression Tube 12F FDA UDI

Identifiers

Catalog Number
000734 FDA UDI
Primary DI / UDI-DI
00801741051685 FDA UDI
FDA Product Code
KNT FDA UDI
GMDN Term
Gastrojejunostomy tube FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5980 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

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
Catheter Gauge — 12 French FDA UDI
Length — 89 Centimeter FDA UDI

Bard Wire-Guided Jejunal Feeding/Gastric Decompression Tube by Bard Access Systems, Inc. — Class II — FDA UDI — listed in FDA GUDID

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

Manufacturer
Bard Access Systems, Inc.

Sources (1)

  • FDA UDI 383873de-a357-4e32-95bb-9d4e3c66f4f9 37 fields · synced Jun 9, 2026