Skip to content

Ventlab FH603007

by Ventlab Corp.

Ventlab FH603007 is a Class II device made by Ventlab Corp., listed in FDA GUDID since 17 Jul 2023 (UDI-DI 10889483081860), 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 Number10889483081860 UDI-DI Date17 Jul 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  • Withdrawn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
Microbial medical gas filter, single-use
Model / Ref / Catalog
FH603007
Primary DI / UDI-DI
10889483081860
FDA product code
CAH
GMDN term
Microbial medical gas filter, single-use
Device class
Class II
Regulation number
868.5260
GUDID distribution status
In Commercial Distribution
Size
Outer Diameter — 22 Millimeter

Related devices

Category: Microbial medical gas filter, single-use

Similar devices in this category

Other devices filed under Microbial medical gas filter, single-use.

Other devices from Ventlab Corp.

See all devices from Ventlab Corp. →

Properties

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