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Veoflo High Flow Nasal Cannula Small Adult Plus Adapter

FDA UDI

Class I (US FDA UDI)

by Flexicare Medical Limited

Identity

Trade Name
Veoflo High Flow Nasal Cannula Small Adult Plus Adapter FDA UDI
Generic Name
Nasal oxygen cannula, basic FDA UDI
Model / Reference
032-10-170U FDA UDI

Identifiers

Primary DI / UDI-DI
05055788770862 FDA UDI
FDA Product Code
CAT FDA UDI
GMDN Term
Nasal oxygen cannula, basic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
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

Yes

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, basic

A semi-rigid tube with nasal prongs designed to be inserted into the nostrils of a patient, and held in place with a headstrap, to administer oxygen (O2). It is commonly known as "nasal prongs". This device has been certified by regulatory agencies for use in critical care settings.

Similar devices

Also classified as Nasal oxygen cannula, basic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Flexicare Medical Limited

Sources (1)

  • FDA UDI 3fe43e50-1b01-4d87-9c22-8c1dd10d0fd2 32 fields · synced Oct 6, 2026