← 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
Absorbent underpad, non-antimicrobial, single-use FDA UDI
Device Name
Disposable Underpads 23in X 36IN (58.4cm X 91.4cm) 54g FDA UDI
Model / Reference
11402 FDA UDI
Description
Disposable Underpads 23in X 36IN (58.4cm X 91.4cm) 54g FDA UDI

Identifiers

Primary DI / UDI-DI
00368001114028 FDA UDI
FDA Product Code
KME FDA UDI
GMDN Term
Absorbent underpad, non-antimicrobial, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6060 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Absorbent underpad, non-antimicrobial, single-use

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

Similar devices

Also classified as Absorbent underpad, non-antimicrobial, single-use.

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 5c8414c1-2d84-4204-ad5b-162153d7d660 33 fields · synced Jun 1, 2026