Skip to content

gSource gS 51.7750

by Gsource, LLC.

Ref gS 51.7750

gSource gS 51.7750 is a bone curette (EU MDR Class I; FDA Class I; FDA product code FZS, Curette, Surgical, General Use) made by Gsource, LLC., registered in EUDAMED on 26 May 2026 (Basic UDI-DI 08403142SCRAPINGPD) and listed in FDA GUDID since 7 Aug 2026 (UDI-DI 00840314270290), active as of 25 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing GUDID Number00840314270290 UDI-DI Date7 Aug 2026ListedStatusListed GUDID: in commercial distribution
European UnionCE/MDR EUDAMED Number08403142SCRAPINGPD Basic UDI-DI 00840314270290UDI-DIDate26 May 2026RegisteredStatusActive

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08403142SCRAPINGPD registered 26 May 2026 Active
  • FDA GUDID UDI-DI 00840314270290 listed 7 Aug 2026 Listed

Timeline

2 dated events

  1. Registered EUDAMED 08403142SCRAPINGPD
  2. Listed FDA GUDID 00840314270290

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
gCurette, Rake, 15", Straight, 10mm, with Silicone Handle, Black, Threaded EUDAMED
gSource GUDID
Generic name
Bone curette, reusable
Device name
Scraping
Model / Ref / Catalog
gS 51.7750
Primary DI / UDI-DI
00840314270290
Basic UDI-DI
08403142SCRAPINGPD
Direct marketing DI
00840314270290
FDA product code
FZS
EMDN code
L0901 Orthopaedic surgery spoons and curettes, reusable
GMDN term
Bone curette, reusable
Device class
Class I
Regulation number
878.4800
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices in this category

Other devices filed under ORTHOPAEDIC SURGERY SPOONS AND CURETTES, REUSABLE.

Other devices from Gsource, LLC.

See all devices from Gsource, LLC. →

Properties

  • Sterilise before use
  • Reusable
  • Premarket exempt
  • Lot / batch number
Other properties (21, all answered No)