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Guide Full Anchor Driver Engine HARSEGF

by Ossvis Co., Ltd.

Guide Full Anchor Driver Engine HARSEGF is a Class I device made by Ossvis Co., Ltd., listed in FDA GUDID since 15 Dec 2025 (UDI-DI 08809918274129), 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 Number08809918274129 UDI-DI Date15 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  • Withdrawn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
Guide Full Anchor Driver Engine
Generic name
Surgical screwdriver, reusable
Model / reference
HARSEGF
Primary DI / UDI-DI
08809918274129
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

Similar devices

Other devices filed under FDA product code NDP (Accessories, Implant, Dental, Endosseous).

Other devices from Ossvis Co., Ltd.

See all devices from Ossvis Co., Ltd. →

Properties

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