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Trusilk E5E75CX26P

by Healthium Medtech Limited

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 Number08903837402363 UDI-DI Date19 Aug 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  • Withdrawn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
Trusilk
Generic Name
Silk suture
Model / Reference
E5E75CX26P
Primary DI / UDI-DI
08903837402363
FDA Product Code
GAP
GMDN Term
Silk suture
Device Class
Class II
Regulation Number
878.5030
GUDID distribution status
In Commercial Distribution

Other devices from Healthium Medtech Limited

  • Trusynth

    Class III

  • Sironix

    Class I

  • Clinifibre

    Class IIb

  • Trusynth Fast

    Class III

  • Trugldye

    Class III

  • Trusilk

    Class III

See all devices from Healthium Medtech Limited →

Properties

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

Other properties (8)

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