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Trewavis Surgical Sbt 200

by Trewavis Surgical Instruments Pty Ltd

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 Number09340254029442 UDI-DI Date13 Oct 2022ListedStatusListed 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  • Withdrawn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
Trewavis Surgical
Generic Name
Open-surgery biopsy forceps, reusable
Model / Ref / Catalog
SBT 200
Primary DI / UDI-DI
09340254029442
FDA Product Code
FCL
GMDN Term
Open-surgery biopsy forceps, reusable
Device Class
Class I
Regulation Number
876.1075
GUDID distribution status
In Commercial Distribution

Related devices

Category: Open-surgery biopsy forceps, reusable

Other devices from Trewavis Surgical Instruments Pty Ltd

Properties

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

Other properties (9)

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