← Back to catalogue

unimed

FDA UDI

Class I (US FDA UDI)

by Unimed Medical Supplies, Inc.

Identity

Trade Name
unimed FDA UDI
Generic Name
Nasal oxygen cannula, carbon-dioxide-sampling FDA UDI
Device Name
Carbon dioxide nasal oxygen tube/Adult FDA UDI
Model / Reference
MCUET2N-UMNC-CO2-A FDA UDI
Description
Carbon dioxide nasal oxygen tube/Adult FDA UDI

Identifiers

Primary DI / UDI-DI
06945664888639 FDA UDI
FDA Product Code
CAT FDA UDI
GMDN Term
Nasal oxygen cannula, carbon-dioxide-sampling 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Nasal oxygen cannula, carbon-dioxide-sampling

unimed by Unimed Medical Supplies, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasal oxygen cannula, carbon-dioxide-sampling.

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

Sources (1)

  • FDA UDI cae09213-caa2-45fe-a0bc-cdafddea1b8c 33 fields · synced May 30, 2026