← Back to catalogue

Comfort Soft Plus CO2 Sampling Nasal Cannula

FDA UDI

Class I (US FDA UDI)

by Westmed, Inc.

Identity

Trade Name
Comfort Soft Plus CO2 Sampling Nasal Cannula FDA UDI
Generic Name
Oxygen administration tubing FDA UDI
Device Name
Adult nasal Cannula, V-Cut 10' O2/CO2 0.045 ID sampling line w/male luer FDA UDI
Model / Reference
0861 FDA UDI
Description
Adult nasal Cannula, V-Cut 10' O2/CO2 0.045 ID sampling line w/male luer FDA UDI

Identifiers

Primary DI / UDI-DI
00709078001499 FDA UDI
FDA Product Code
CAI FDA UDI
GMDN Term
Oxygen administration tubing FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5240 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: Oxygen administration tubing

Comfort Soft Plus CO2 Sampling Nasal Cannula by Westmed, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Oxygen administration tubing.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Westmed, Inc.

Sources (1)

  • FDA UDI 5a7d9129-7d0f-491a-b28c-d644aec2f972 33 fields · synced May 30, 2026