← Back to catalogue

Flexicare

FDA UDI

Class II (US FDA UDI)

by Flexicare Medical Limited

Identity

Trade Name
Flexicare FDA UDI
Generic Name
Nasal oxygen cannula, carbon-dioxide-sampling FDA UDI
Device Name
Dual Adult Oral Nasal Cannula 7ft O2 Delivery/CO2 Monitoring, Filter, Microstream Luer, M-M Adapter FDA UDI
Model / Reference
032-10-180/1U FDA UDI
Description
Dual Adult Oral Nasal Cannula 7ft O2 Delivery/CO2 Monitoring, Filter, Microstream Luer, M-M Adapter FDA UDI

Identifiers

Primary DI / UDI-DI
05055931101024 FDA UDI
FDA Product Code
CCK FDA UDI
CAT 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
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

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

Flexicare 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 e259b758-ea3e-4a19-a3a2-d066663e17a9 33 fields · synced May 30, 2026