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Nasal-Aire II

FDA UDI

Class II (US FDA UDI)

by Innomed Technologies

Identity

Trade Name
Nasal-Aire II FDA UDI
Generic Name
CPAP/BPAP nasal mask, single-use FDA UDI
Device Name
Nasal-Aire II Critical Care – LG (with Port) FDA UDI
Model / Reference
CLG5P FDA UDI
Description
Nasal-Aire II Critical Care – LG (with Port) FDA UDI

Identifiers

Catalog Number
CLG5P FDA UDI
Primary DI / UDI-DI
00833224000880 FDA UDI
FDA Product Code
BZD FDA UDI
GMDN Term
CPAP/BPAP nasal 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

Category: CPAP/BPAP nasal mask, single-use

Nasal-Aire II by Innomed Technologies — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 542c8bb5-a733-4890-85e9-eabab813d5b6 35 fields · synced May 30, 2026