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AnyPlus® GS114-0659

by GS Medical Co., Ltd.

AnyPlus® GS114-0659 is a Class I device made by GS Medical Co., Ltd., listed in FDA GUDID since 22 Sep 2020 (UDI-DI 08806395478897), 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 Number08806395478897 UDI-DI Date22 Sep 2020ListedStatusListed 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  • Withdrawn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
AnyPlus®
Generic name
Bone tap, reusable
Model / Ref / Catalog
GS114-0659
Primary DI / UDI-DI
08806395478897
FDA product code
HWX
GMDN term
Bone tap, reusable
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Bone tap, reusable

Other devices from GS Medical Co., Ltd.

See all devices from GS Medical Co., Ltd. →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Serial number
  • Manufacturing date
Other properties (9, all answered No)