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CO2 Sampling Nasal Cannula 72` w/Female Luer

FDA UDI

Class I (US FDA UDI)

by Westmed, Inc.

Identity

Trade Name
CO2 Sampling Nasal Cannula 72` w/Female Luer FDA UDI
Generic Name
Oxygen administration tubing FDA UDI
Device Name
CO2 Sampling Nasal Cannula 72` w/Female Luer FDA UDI
Model / Reference
0872 FDA UDI
Description
CO2 Sampling Nasal Cannula 72` w/Female Luer FDA UDI

Identifiers

Primary DI / UDI-DI
00709078002519 FDA UDI
FDA Product Code
CAT FDA UDI
CCK FDA UDI
GMDN Term
Oxygen administration tubing FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5340 FDA UDI
868.1400 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

CO2 Sampling Nasal Cannula 72` w/Female Luer 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 2daec028-78fb-4e90-941e-62d8bcb12856 34 fields · synced Jun 6, 2026