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T01 Fixture

by OSSTEM IMPLANT Co., Ltd. 23 variants

Part of a family of 60 devices: see the family page

Ref T015010S

T01 Fixture (T015010S) is a Class IIb device made by Osstem Implant Co., Ltd, registered in EUDAMED on 26 Feb 2026 (Basic UDI-DI 88000406MSAP), 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 Number88000406MSAP Basic UDI-DI 08800271298975UDI-DIDate26 Feb 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
MS Implant System
Model / reference
T015010S
Primary DI / UDI-DI
08800271298975
Basic UDI-DI
88000406MSAP
EMDN code
P01020101 Dental implants
Device class
Class IIb
EU registration type
Standard device
EU market of registration
Czechia

Manufacturer details

EUDAMED SRN
KR-MF-000020006
Authorised representative
Obelis s.a. BE-AR-000000106

Similar devices in this category

Other devices filed under DENTAL IMPLANTS.

Other devices from Osstem Implant Co., Ltd

See all devices from Osstem Implant Co., Ltd →

Properties

  • Supplied sterile
  • Implantable
  • Sutures
Other properties (12, all answered No)