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Flexicare

FDA UDI

Class II (US FDA UDI)

by Flexicare Medical Limited

Identity

Trade Name
Flexicare FDA UDI
Generic Name
Gas-sampling/monitoring respiratory tubing, single-use FDA UDI
Device Name
CapnoCare Capnography Connector 10ft Extended Use, Filter, Microstream Compatible FDA UDI
Model / Reference
010-762LU FDA UDI
Description
CapnoCare Capnography Connector 10ft Extended Use, Filter, Microstream Compatible FDA UDI

Identifiers

Primary DI / UDI-DI
05055931127918 FDA UDI
FDA Product Code
CCK FDA UDI
GMDN Term
Gas-sampling/monitoring respiratory tubing, single-use 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

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: Gas-sampling/monitoring respiratory tubing, single-use

Flexicare by Flexicare Medical Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gas-sampling/monitoring respiratory tubing, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3a6a3191-ba73-40a6-a3d9-c89da0b13943 33 fields · synced Jun 6, 2026