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Dual Nare Nasal Cannulae, Female Luer W/Filter, 7ft O2 Tube

FDA UDI

Class I (US FDA UDI)

by Flexicare Medical Limited

Identity

Trade Name
DUAL NARE NASAL CANNULAE,FEMALE LUER W/FILTER, 7FT O2 TUBE FDA UDI
Generic Name
Nasal oxygen cannula, carbon-dioxide-sampling FDA UDI
Model / Reference
032-10-126AU FDA UDI

Identifiers

Primary DI / UDI-DI
05055788755487 FDA UDI
FDA Product Code
CAT FDA UDI
CCK 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
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

Yes

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 Nare Nasal Cannulae, Female Luer W/Filter, 7ft O2 Tube by Flexicare Medical Limited — Class I — FDA UDI — listed in FDA GUDID

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 69f4e0b6-7bf6-4477-a8f9-d5190f2c18cb 32 fields · synced Jun 8, 2026