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EZ Post Abutment

by MegaGen Implant Co., Ltd. 87 variants

Part of a family of 586 devices: see the family page

Ref AOEP6017NT

EZ Post Abutment (AOEP6017NT) is a Class IIb device made by Megagen Implant Co., Ltd., registered in EUDAMED on 5 Sep 2026 (Basic UDI-DI 880972899863F), active as of 24 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number880972899863F Basic UDI-DI 08800292999936UDI-DIDate5 Sep 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device name
EZ Post Abutment
Model / reference
AOEP6017NT
Primary DI / UDI-DI
08800292999936
Basic UDI-DI
880972899863F
EMDN code
P01020101 Dental implants
Device class
Class IIb
EU registration type
Standard device
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
KR-MF-000009885
Authorised representative
MDSS GmbH DE-AR-000005430

Similar devices in this category

Other devices filed under DENTAL IMPLANTS.

Other devices from Megagen Implant Co., Ltd.

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

Properties

  • Sterilise before use
  • Implantable
  • Sutures
Other properties (12, all answered No)