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Ventlab

FDA UDI

Class I (US FDA UDI)

by Ventlab Corp.

Identity

Trade Name
Ventlab FDA UDI
Generic Name
Nasal oxygen cannula, basic FDA UDI
Device Name
INFANT CANNULA WITH 7' TUBING AND FITS-ALL FDA UDI
Model / Reference
1307F FDA UDI
Description
INFANT CANNULA WITH 7' TUBING AND FITS-ALL FDA UDI

Identifiers

Catalog Number
1307F FDA UDI
Primary DI / UDI-DI
10889483074275 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 7 Centimeter FDA UDI

Category: Nasal oxygen cannula, basic

Ventlab by Ventlab Corp. — 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
Ventlab Corp.

Sources (1)

  • FDA UDI eb9e7760-7303-412f-827b-64dfffea1ac9 36 fields · synced Jun 8, 2026