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Adult CO2 /O2 Mask

FDA UDI

Class I (US FDA UDI)

by Westmed, Inc.

Identity

Trade Name
Adult CO2 /O2 Mask FDA UDI
Generic Name
Nasal oxygen cannula, carbon-dioxide-sampling FDA UDI
Device Name
Pediatric Elongated CO2/O2 Mask 7' Tubing w/ Threaded Nut, Swivel GSE, 10' x 0.38" ID x .107" OD, Reflective Luer Connectors FDA UDI
Model / Reference
0931 FDA UDI
Description
Pediatric Elongated CO2/O2 Mask 7' Tubing w/ Threaded Nut, Swivel GSE, 10' x 0.38" ID x .107" OD, Reflective Luer Connectors FDA UDI

Identifiers

Primary DI / UDI-DI
00709078006876 FDA UDI
FDA Product Code
BSJ FDA UDI
CCK FDA UDI
GMDN Term
Nasal oxygen cannula, carbon-dioxide-sampling FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5550 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

Adult CO2 /O2 Mask 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 fee35355-3a72-42f4-a36d-2c4cce5f83d0 34 fields · synced Jun 1, 2026