← Back to catalogue

AmerisourceBergen

FDA UDI

Class I (US FDA UDI)

by Bp Pharmaceuticals Laboratories Unlimited Company

Identity

Trade Name
AmerisourceBergen FDA UDI
Generic Name
General-purpose surgical sponge FDA UDI
Device Name
Brown Gauze Roll 3 in X 5 yd, non-sterile FDA UDI
Model / Reference
10336 FDA UDI
Description
Brown Gauze Roll 3 in X 5 yd, non-sterile FDA UDI

Identifiers

Primary DI / UDI-DI
00368001103367 FDA UDI
FDA Product Code
NAB FDA UDI
GMDN Term
General-purpose surgical sponge FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4014 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

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General-purpose surgical sponge

AmerisourceBergen by Bp Pharmaceuticals Laboratories Unlimited Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose surgical sponge.

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

Sources (1)

  • FDA UDI bfdb5666-eb5a-40f7-8c83-40fc4f9446ac 33 fields · synced May 29, 2026