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AmerisourceBergen

FDA UDI

Class I (US FDA UDI)

by Bp Pharmaceuticals Laboratories Unlimited Company

Identity

Trade Name
AmerisourceBergen FDA UDI
Generic Name
Inoculating tool IVD, manual FDA UDI
Device Name
Fecal Loops Disposable Pediatric Size FDA UDI
Model / Reference
11502 FDA UDI
Description
Fecal Loops Disposable Pediatric Size FDA UDI

Identifiers

Primary DI / UDI-DI
00368001115025 FDA UDI
FDA Product Code
LXG FDA UDI
GMDN Term
Inoculating tool IVD, manual FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2050 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: Inoculating tool IVD, manual

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

Similar devices

Also classified as Inoculating tool IVD, manual.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 40835638-dbde-4e22-91a9-9f81390dd642 33 fields · synced May 31, 2026