← Back to catalogue

Dual Medium Mask

FDA UDI

Class II (US FDA UDI)

by Flexicare Medical Limited

Identity

Trade Name
Dual Medium Mask FDA UDI
Generic Name
Nasal oxygen cannula, carbon-dioxide-sampling FDA UDI
Device Name
7ft Combined O2 Delivery/CO2 Monitoring Filter with Microstream Type Luer Connector FDA UDI
Model / Reference
032-10-192U FDA UDI
Description
7ft Combined O2 Delivery/CO2 Monitoring Filter with Microstream Type Luer Connector FDA UDI

Identifiers

Primary DI / UDI-DI
05055788781875 FDA UDI
FDA Product Code
CCK FDA UDI
GMDN Term
Nasal oxygen cannula, carbon-dioxide-sampling FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.1400 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

No

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Nasal oxygen cannula, carbon-dioxide-sampling

Dual Medium Mask by Flexicare Medical Limited — Class II — 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 c82545a4-ea66-4d12-aece-e9898a78948e 33 fields · synced May 30, 2026