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Dual Nasal Cannula Adult, Male Luer W/ Slip Filter 7ft

FDA UDI

Class II (US FDA UDI)

by Flexicare Medical Limited

Identity

Trade Name
DUAL NASAL CANNULA ADULT, MALE LUER W/ SLIP FILTER 7FT FDA UDI
Generic Name
Nasal oxygen cannula, carbon-dioxide-sampling FDA UDI
Model / Reference
032-10-125BU FDA UDI

Identifiers

Primary DI / UDI-DI
05055788716495 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, basicNasal oxygen cannula, carbon-dioxide-sampling

Dual Nasal Cannula Adult, Male Luer W/ Slip Filter 7ft 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

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Manufacturer

Sources (1)

  • FDA UDI e8b8eb00-6518-4cfe-9157-5a9624ef08e2 32 fields · synced Jun 8, 2026