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Bf

FDA UDI

Class II (US FDA UDI)

by Allied Medical LLC

Identity

Trade Name
BF FDA UDI
Generic Name
Ventilator breathing circuit, single-use FDA UDI
Device Name
VENT CIRCUIT TUBING HAN- FDA UDI
Model / Reference
64600 FDA UDI
Description
VENT CIRCUIT TUBING HAN- FDA UDI

Identifiers

Primary DI / UDI-DI
00026072025024 FDA UDI
FDA Product Code
GAZ FDA UDI
GMDN Term
Ventilator breathing circuit, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 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

No

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: Ventilator breathing circuit, single-use

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

Similar devices

Also classified as Ventilator breathing circuit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Allied Medical LLC

Sources (1)

  • FDA UDI dce75a6c-37c0-47d4-b3f8-7e5347549ff0 33 fields · synced May 30, 2026