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Ti-Base

by ARUM DENTISTRY Co., Ltd. 300 variants

Part of a family of 1,915+ devices: see the family page

Ref LINH011P

Ti-Base (LINH011P) is a Class IIb device made by ARUM DENTISTRY Co., Ltd., registered in EUDAMED on 1 Jun 2026 (Basic UDI-DI 88000557CADCAMAY), active as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number88000557CADCAMAY Basic UDI-DI 08800055770598UDI-DIDate1 Jun 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Abutment and Abutment screw
Model / reference
LINH011P
Primary DI / UDI-DI
08800055770598
Basic UDI-DI
88000557CADCAMAY
EMDN code
P01020180 Dental implants - accessories
Device class
Class IIb
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
KR-MF-000009313
Authorised representative
MedNet EC-REP IIb GmbH DE-AR-000011192

Similar devices in this category

Other devices filed under DENTAL IMPLANTS - ACCESSORIES.

Other devices from ARUM DENTISTRY Co., Ltd.

See all devices from ARUM DENTISTRY Co., Ltd. →

Properties

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