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Bard® Levin Duodenal Tube

FDA UDI

Class II (US FDA UDI)

by C. R. Bard, Inc.

Identity

Trade Name
Bard® Levin Duodenal Tube FDA UDI
Generic Name
Gastric lavage kit FDA UDI
Device Name
Bard® Levin Duodenal Tube FDA UDI
Model / Reference
0005550 FDA UDI
Description
Bard® Levin Duodenal Tube FDA UDI

Identifiers

Catalog Number
0005550 FDA UDI
Primary DI / UDI-DI
00801741076701 FDA UDI
FDA Product Code
FRQ 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

No

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
Sterilization Method
Ethylene Oxide FDA UDI

Dimensions & Sizes

Size
Length — 48 Inch FDA UDI
Catheter Gauge — 20 French FDA UDI

Category: Gastric lavage kit

Bard® Levin Duodenal Tube 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 de085579-99a2-4702-b2f3-23e8825f4268 36 fields · synced Jun 8, 2026