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Wisp

FDA UDI

Class II (US FDA UDI)

by Respironics, Inc.

Identity

Trade Name
Wisp FDA UDI
Generic Name
CPAP/BPAP nasal mask, reusable FDA UDI
Device Name
Wisp Mask, Clear Frame, with Headgear, Extra Large, International FDA UDI
Model / Reference
Wisp Mask, Exra Large, Clear Frame, w/Headgear, INTL FDA UDI
Description
Wisp Mask, Clear Frame, with Headgear, Extra Large, International FDA UDI

Identifiers

Catalog Number
1093926 FDA UDI
Primary DI / UDI-DI
00606959040045 FDA UDI
FDA Product Code
BZD FDA UDI
GMDN Term
CPAP/BPAP nasal 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 nasal mask, reusable

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

Similar devices

Also classified as CPAP/BPAP nasal 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 f4e17507-7f15-437a-908f-4712ab28945c 36 fields · synced Jun 1, 2026