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BiPAP

FDA UDI

Class II (US FDA UDI)

by Respironics, Inc.

Identity

Trade Name
BiPAP FDA UDI
Generic Name
Ventilator breathing circuit, single-use FDA UDI
Device Name
CIRCUIT FILTER, DISPOSABLE EXHALATION PORT WITH FILTERED EXHALATION PORT FILTER, SINGLE, INTERNATIONAL FDA UDI
Model / Reference
Circuit Filter Disp Exhal Port with FEP Filter, Single, INTL FDA UDI
Description
CIRCUIT FILTER, DISPOSABLE EXHALATION PORT WITH FILTERED EXHALATION PORT FILTER, SINGLE, INTERNATIONAL FDA UDI

Identifiers

Catalog Number
1073949 FDA UDI
Primary DI / UDI-DI
00606959042377 FDA UDI
FDA Product Code
MNT FDA UDI
GMDN Term
Ventilator breathing circuit, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5895 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Ventilator breathing circuit, single-use

BiPAP by Respironics, Inc. — 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
Respironics, Inc.

Sources (1)

  • FDA UDI cdb49337-49f5-4720-a960-592f869012cf 36 fields · synced Jun 8, 2026