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Ventlab 3004HZ

by Ventlab Corp.

Ventlab 3004HZ is a Class II device made by Ventlab Corp., listed in FDA GUDID since 21 Mar 2023 (UDI-DI 10889483165515), 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 Number10889483165515 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  • Withdrawn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
Airway pressure monitor, non-powered
Model / Ref / Catalog
3004HZ
Primary DI / UDI-DI
10889483165515
FDA product code
NHK
GMDN term
Airway pressure monitor, non-powered
Device class
Class II
Regulation number
868.5905
GUDID distribution status
In Commercial Distribution
Size
Total Volume — 0.5 Liter

Related devices

Category: Airway pressure monitor, non-powered

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Other devices filed under Airway pressure monitor, non-powered.

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Properties

  • Single use
  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)