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Ventlab VR1400-40

by Ventlab Corp.

Ventlab VR1400-40 is a Class I device made by Ventlab Corp., listed in FDA GUDID since 2 Jun 2023 (UDI-DI 10889483098578), 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 Number10889483098578 UDI-DI Date2 Jun 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  • Withdrawn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
Anaesthesia face mask, single-use
Model / Ref / Catalog
VR1400-40
Primary DI / UDI-DI
10889483098578
FDA product code
BSJ
GMDN term
Anaesthesia face mask, single-use
Device class
Class I
Regulation number
868.5550
GUDID distribution status
In Commercial Distribution

Related devices

Category: Anaesthesia face mask, single-use

Similar devices in this category

Other devices filed under Anaesthesia face mask, single-use.

Other devices from Ventlab Corp.

See all devices from Ventlab Corp. →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)