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Comfort Soft Plus

FDA UDI

Class I (US FDA UDI)

by Westmed, Inc.

Identity

Trade Name
Comfort Soft Plus FDA UDI
Generic Name
Nasal oxygen cannula, carbon-dioxide-sampling FDA UDI
Device Name
Adult Oral/Nasal Sampling Cannula 10' O2CO2 Tubing w/male luer, 2" pigtail w/female luers FDA UDI
Model / Reference
0430 FDA UDI
Description
Adult Oral/Nasal Sampling Cannula 10' O2CO2 Tubing w/male luer, 2" pigtail w/female luers FDA UDI

Identifiers

Primary DI / UDI-DI
00709078001550 FDA UDI
FDA Product Code
CAT FDA UDI
GMDN Term
Nasal oxygen cannula, carbon-dioxide-sampling FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5340 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: Nasal oxygen cannula, carbon-dioxide-sampling

Comfort Soft Plus by Westmed, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasal oxygen cannula, carbon-dioxide-sampling.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Westmed, Inc.

Sources (1)

  • FDA UDI c17bde2b-5cbf-410c-b983-cbaa99b4a3f4 33 fields · synced May 30, 2026