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Bard® Levin Duodenal Tubes

FDA UDI

Class II (US FDA UDI)

by C. R. Bard, Inc.

Identity

Trade Name
Bard® Levin Duodenal Tubes FDA UDI
Generic Name
Gastric lavage kit FDA UDI
Device Name
Bard® Levin Duodenal Tubes FDA UDI
Model / Reference
8029630 FDA UDI
Description
Bard® Levin Duodenal Tubes FDA UDI

Identifiers

Catalog Number
8029630 FDA UDI
Primary DI / UDI-DI
10801741122498 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 — 18 French FDA UDI

Category: Gastric lavage kit

Bard® Levin Duodenal Tubes 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 2aa2e81d-e9bd-4b70-87aa-38d6dcd2b937 36 fields · synced Jun 8, 2026