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Reamer T-handle AR-902-13

by G21 SRL

Reamer T-handle AR-902-13 is a Class I device made by G21 SRL, listed in FDA GUDID since 19 Dec 2025 (UDI-DI 08058964729262), 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 Number08058964729262 UDI-DI Date19 Dec 2025ListedStatusListed 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  • Withdrawn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
Reamer T-handle
Generic name
Shoulder revision prosthesis trial
Model / reference
AR-902-13
Primary DI / UDI-DI
08058964729262
FDA product code
HWT
GMDN term
Shoulder revision prosthesis trial
Device class
Class I
Regulation number
888.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices

Other devices filed under FDA product code HWT (Template).

Other devices from G21 SRL

See all devices from G21 SRL →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)