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LinkUS Drain 1

by Interlinked AB

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

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 Number17350128050006 UDI-DI Date31 May 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
LinkUS Drain
Generic Name
Luer/Luer breakaway connector
Model / Reference
LinkUS Drain 1
Primary DI / UDI-DI
17350128050006
FDA Product Code
GBX
GMDN Term
Luer/Luer breakaway connector
Device Class
Class I
Regulation Number
878.4200
GUDID distribution status
In Commercial Distribution

Other devices from Interlinked AB

  • ReLink Drain

    Class I

  • ReLink IV

    Class IIa

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (8)

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