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Comfort Soft Plus, Premature

FDA UDI

Class I (US FDA UDI)

by Westmed, Inc.

Identity

Trade Name
Comfort Soft Plus,Premature FDA UDI
Generic Name
Nasal oxygen cannula, basic FDA UDI
Device Name
Comfort Soft Plus,Premature Soft Tipped Cannula,W/7'KROT&TN FDA UDI
Model / Reference
0153 FDA UDI
Description
Comfort Soft Plus,Premature Soft Tipped Cannula,W/7'KROT&TN FDA UDI

Identifiers

Primary DI / UDI-DI
00709078003851 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
Not 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

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Westmed, Inc.

Sources (1)

  • FDA UDI df9c0bfd-217a-4e8e-99ba-1df1e53d8159 34 fields · synced Jun 1, 2026