24M - Mid America Energy BBP

FDA UDI

Class II (US FDA UDI)

by Certified Safety Manufacturing, Inc.

Identity

Trade Name: 24M - Mid America Energy BBP FDA UDI
Generic Name: Non-rebreathing valve, single-use FDA UDI
Device Name: 24M - Mid America Energy BBP FDA UDI
Model / Reference: FK208-308 FDA UDI
Description: 24M - Mid America Energy BBP FDA UDI

Identifiers

Catalog Number: FK208-308 FDA UDI
Primary DI / UDI-DI: 00766588083087 FDA UDI
FDA Product Code: CBP FDA UDI
LRR FDA UDI
GMDN Term: Non-rebreathing valve, single-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 868.5870 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: First aid kit, medicated Non-rebreathing valve, single-use Cardiopulmonary resuscitation mask, single-use

24M - Mid America Energy BBP by Certified Safety Manufacturing, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Certified Safety Manufacturing, Inc.

Sources (1)

FDA UDI 989bc27c-46a8-45f6-b64e-037755b0c558 35 fields · synced Jun 6, 2026