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TS DR Abutment

by OSSTEM IMPLANT Co., Ltd. 120 variants

Ref TSDSRA609R

TS DR Abutment (TSDSRA609R) is a Class IIb device made by Osstem Implant Co., Ltd, registered in EUDAMED on 26 Feb 2026 (Basic UDI-DI 88000406CSHAKX), active as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number88000406CSHAKX Basic UDI-DI 08809917151742UDI-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  • Withdrawn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
Dental Abutment System(STERILE)
Model / reference
TSDSRA609R
Primary DI / UDI-DI
08809917151742
Basic UDI-DI
88000406CSHAKX
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

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Properties

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