Bf

FDA UDI

Class I (US FDA UDI)

by Allied Medical LLC

Identity

Trade Name: BF FDA UDI
Generic Name: Non-fixed medical gas cylinder regulator FDA UDI
Device Name: REG O2 50PSI 0-25 DISS/OHMEDA FDA UDI
Model / Reference: 21225 FDA UDI
Description: REG O2 50PSI 0-25 DISS/OHMEDA FDA UDI

Identifiers

Primary DI / UDI-DI: 00026072023839 FDA UDI
FDA Product Code: CAN FDA UDI
GMDN Term: Non-fixed medical gas cylinder regulator FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 868.2700 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Non-fixed medical gas cylinder regulator

Bf by Allied Medical LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-fixed medical gas cylinder regulator.

Ohio — Ohio Medical LLC · Class I
Patient Loading Utility System (PLUS) — LIFEPORT, LLC. · Class I
CarboJet® CO2 Bone Lavage System — Kinamed, Inc. · Class II
Ohio — Ohio Medical LLC · Class I
Patient Loading Utility System (PLUS) — LIFEPORT, LLC. · Class I
Ohio — Ohio Medical LLC · Class I
Ohio — Ohio Medical LLC · Class I
CarboJet® CO2 Bone Lavage System — Kinamed, Inc. · Class II

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 I	Pending data

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Allied Medical LLC

Sources (1)

FDA UDI 21b83316-70e4-4832-8bfd-646725ab0461 33 fields · synced May 29, 2026