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Ventlab 1215F

by Ventlab Corp.

Ventlab 1215F is a Class I device made by Ventlab Corp., listed in FDA GUDID since 21 Mar 2023 (UDI-DI 10889483169049), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10889483169049 UDI-DI Date21 Mar 2023ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Ventlab
Generic name
Nasal oxygen cannula, basic
Model / Ref / Catalog
1215F
Description
Pediatric O2 Cannula with 15' Tubing & Fits-All Connector
Primary DI / UDI-DI
10889483169049
FDA product code
CAT
GMDN term
Nasal oxygen cannula, basic
Device class
Class I
Regulation number
868.5340
GUDID distribution status
In Commercial Distribution
Size
Length — 15 Centimeter

Related devices

Category: Nasal oxygen cannula, basic

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Other devices filed under Nasal oxygen cannula, basic.

Other devices from Ventlab Corp.

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Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)