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Handpiece Driver HD120

by Surgident

Handpiece Driver HD120 is a Class I device made by Surgident, listed in FDA GUDID since 3 Mar 2023 (UDI-DI 08800041039296), 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 Number08800041039296 UDI-DI Date3 Mar 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  • Withdrawn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
Handpiece Driver
Generic name
Surgical screwdriver, reusable
Model / reference
HD120
Primary DI / UDI-DI
08800041039296
FDA product code
NDP
GMDN term
Surgical screwdriver, reusable
Device class
Class I
Regulation number
872.3980
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Surgical screwdriver, reusable

Similar devices in this category

Other devices filed under Surgical screwdriver, reusable.

Other devices from Surgident

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Properties

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