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PerforMax

FDA UDI

Class II (US FDA UDI)

by Respironics, Inc.

Identity

Trade Name
PerforMax FDA UDI
Generic Name
CPAP/BPAP face mask, reusable FDA UDI
Device Name
Performax with Entrainment Elbow, Leak 2, Multi Patient Use, USA, Large FDA UDI
Model / Reference
Performax Mask w/EE Leak 2, Multi Patient Use, Large, USA FDA UDI
Description
Performax with Entrainment Elbow, Leak 2, Multi Patient Use, USA, Large FDA UDI

Identifiers

Catalog Number
1047427 FDA UDI
Primary DI / UDI-DI
00606959011786 FDA UDI
FDA Product Code
BZD FDA UDI
GMDN Term
CPAP/BPAP face mask, 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

No

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: CPAP/BPAP face mask, reusable

PerforMax by Respironics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as CPAP/BPAP face mask, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Respironics, Inc.

Sources (1)

  • FDA UDI 2463980b-26dc-46d3-88a4-0e3d4a2ccf09 36 fields · synced Jun 8, 2026