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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, single-use FDA UDI
Device Name
Performax Mask, with Standard Elbow, Single Use, Small FDA UDI
Model / Reference
Performax Mask, Single Use w/SE, Small FDA UDI
Description
Performax Mask, with Standard Elbow, Single Use, Small FDA UDI

Identifiers

Catalog Number
1061621 FDA UDI
Primary DI / UDI-DI
00606959007703 FDA UDI
510(k) Number
K092648 FDA UDI
FDA Product Code
CBK FDA UDI
GMDN Term
CPAP/BPAP face mask, 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: CPAP/BPAP face mask, single-use

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, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Respironics, Inc.

Sources (1)

  • FDA UDI 491cfeb2-80b3-4de5-b3d2-fb5ecdb7e780 37 fields · synced Jun 6, 2026