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Anchor Kit KAGAS3001

by Megagen Implant Co. Ltd

Ref KAGAS3001

Anchor Kit KAGAS3001 is a Class I device made by Megagen Implant Co. Ltd, registered in EUDAMED on 1 Sep 2026 (Basic UDI-DI 8809728993732) and listed in FDA GUDID since 26 Jun 2015 (UDI-DI 08806388224500), active as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number8809728993732 Basic UDI-DI 08806388224500UDI-DIDate1 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number08806388224500 UDI-DI Date26 Jun 2015ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 8809728993732 registered 1 Sep 2026 Active
  • FDA GUDID UDI-DI 08806388224500 listed 26 Jun 2015 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 08806388224500
  2. Registered EUDAMED 8809728993732

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  • Withdrawn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
Anchor Kit
Generic name
Dental implant/prosthesis surgical procedure kit
Device name
Surgial Instrument Kit (Anchor Kit)
Model / Ref / Catalog
KAGAS3001
Primary DI / UDI-DI
08806388224500
Basic UDI-DI
8809728993732
FDA product code
NDP
EMDN code
L159016 Dental surgery instrument kits, reusable
GMDN term
Dental implant/prosthesis surgical procedure kit
Device class
Class I
Regulation number
872.3980
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Dental implant/prosthesis surgical procedure kit

Similar devices in this category

Other devices filed under DENTAL SURGERY INSTRUMENT KITS, REUSABLE.

Other devices from Megagen Implant Co., Ltd.

See all devices from Megagen Implant Co., Ltd. →

Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Serial number
  • Manufacturing date
Other properties (18, all answered No)