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Utopia AV

FDA UDI

Class II (US FDA UDI)

by Innomed Technologies

Identity

Trade Name
Utopia AV FDA UDI
Generic Name
CPAP/BPAP face mask, single-use FDA UDI
Device Name
Utopia AV Full Face Mask - SM (with Black Headgear) FDA UDI
Model / Reference
UTO251A FDA UDI
Description
Utopia AV Full Face Mask - SM (with Black Headgear) FDA UDI

Identifiers

Catalog Number
UTO251A FDA UDI
Primary DI / UDI-DI
00833224001023 FDA UDI
FDA Product Code
BZD FDA UDI
GMDN Term
CPAP/BPAP face mask, single-use 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

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: CPAP/BPAP face mask, single-use

Utopia AV by Innomed Technologies — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as CPAP/BPAP face mask, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b3ae8f61-6473-4334-ae6c-cc80e9d388be 36 fields · synced May 29, 2026