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FlowArt® AVV4030Y

by Asset Medikal Tasarim Sanayi Ve Ticaret Anonim Sirketi

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08699443581928 UDI-DI Date13 Feb 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
FlowArt®
Generic Name
Vial/bottle adaptor, non-hermetic
Model / Reference
AVV4030Y
Primary DI / UDI-DI
08699443581928
510(k) Number
FDA Product Code
LHI
GMDN Term
Vial/bottle adaptor, non-hermetic
Device Class
Class II
Regulation Number
880.5440
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K251715)

Other devices from Asset Medikal Tasarim Sanayi Ve Ticaret Anonim Sirketi

See all devices from Asset Medikal Tasarim Sanayi Ve Ticaret Anonim Sirketi →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No