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Adult Comfort Soft Plus

FDA UDI

Class I (US FDA UDI)

by Westmed, Inc.

Identity

Trade Name
Adult Comfort Soft Plus FDA UDI
Generic Name
Nasal oxygen cannula, basic FDA UDI
Device Name
Adult Comfort Soft Plus Cannula w/2' Tubing FDA UDI
Model / Reference
0588 FDA UDI
Description
Adult Comfort Soft Plus Cannula w/2' Tubing FDA UDI

Identifiers

Primary DI / UDI-DI
00709078003806 FDA UDI
FDA Product Code
CAT FDA UDI
GMDN Term
Nasal oxygen cannula, basic 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

Yes

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, basic

Adult 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, basic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Westmed, Inc.

Sources (1)

  • FDA UDI 80c2cbc3-9863-4608-b0de-7383266d412b 34 fields · synced May 30, 2026