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Nasal Cannula

FDA UDI

Class I (US FDA UDI)

by Truer Medical, Inc.

Identity

Trade Name
Nasal Cannula FDA UDI
Generic Name
Nasal oxygen cannula, basic FDA UDI
Device Name
Adult Nasal Cannula w/7' safety channel tubing FDA UDI
Model / Reference
90413 FDA UDI
Description
Adult Nasal Cannula w/7' safety channel tubing FDA UDI

Identifiers

Catalog Number
90413 FDA UDI
Primary DI / UDI-DI
00859290006410 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

Yes

FDA UDI

Category: Nasal oxygen cannula, basic

Nasal Cannula by Truer Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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
Truer Medical, Inc.

Sources (1)

  • FDA UDI f6dee4eb-2976-4634-9e85-ce5c3a15771d 34 fields · synced Jun 1, 2026