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Hex Driver 02-039-90-7000

by Signature Orthopaedics Pty Ltd

Hex Driver 02-039-90-7000 is a Class I device made by Signature Orthopaedics Pty Ltd, listed in FDA GUDID since 20 Feb 2023 (UDI-DI 09348215109592), 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 Number09348215109592 UDI-DI Date20 Feb 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  • Withdrawn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
Hex Driver
Generic name
Orthopaedic implant driver
Model / reference
02-039-90-7000
Primary DI / UDI-DI
09348215109592
FDA product code
HWR
GMDN term
Orthopaedic implant driver
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

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Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)