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BiWaze Cough Dual Lumen Circuit With Trach Adapter

FDA UDI

Class II (US FDA UDI)

by Abmrc LLC

Identity

Trade Name
BiWaze Cough Dual Lumen Circuit With Trach Adapter FDA UDI
Generic Name
Ventilator breathing circuit, reusable FDA UDI
Device Name
BiWaze Cough Dual Lumen Circuit With Trach Adapter FDA UDI
Model / Reference
BC23394 FDA UDI
Description
BiWaze Cough Dual Lumen Circuit With Trach Adapter FDA UDI

Identifiers

Catalog Number
BC23394 FDA UDI
Primary DI / UDI-DI
08500501360020 FDA UDI
FDA Product Code
NHJ FDA UDI
GMDN Term
Ventilator breathing circuit, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5905 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

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ventilator breathing circuit, reusable

BiWaze Cough Dual Lumen Circuit With Trach Adapter by Abmrc LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ventilator breathing circuit, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Abmrc LLC

Sources (1)

  • FDA UDI d721044a-a9dd-4e6c-9aca-3d8a04cfb0d7 35 fields · synced May 31, 2026