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Bard® Baker Jejunostomy Catheter

FDA UDI

Class II (US FDA UDI)

by C. R. Bard, Inc.

Identity

Trade Name
Bard® Baker Jejunostomy Catheter FDA UDI
Generic Name
Gastric lavage kit FDA UDI
Device Name
Bard® Baker Jejunostomy Catheter FDA UDI
Model / Reference
0042500 FDA UDI
Description
Bard® Baker Jejunostomy Catheter FDA UDI

Identifiers

Catalog Number
0042500 FDA UDI
Primary DI / UDI-DI
00801741075674 FDA UDI
FDA Product Code
KNT FDA UDI
GMDN Term
Gastric lavage kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5980 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

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

Yes

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 — 72 Inch FDA UDI
Catheter Gauge — 12 French FDA UDI

Category: Gastric lavage kit

Bard® Baker Jejunostomy Catheter by C. R. Bard, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gastric lavage kit.

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 1ae8ef81-2b77-41e7-afdb-4295fdfc6b02 36 fields · synced May 30, 2026