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Succeeder

by Beijing Succeeder Technology Inc. 12 variants

Ref SF-8200CModel SF-8050, SF-8100, SF-8100C, SF-8200, SF-8200C, SF-8300, SF-9200

Active European Union

CE IVDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number69577052FACAU8 Basic UDI-DI 06957705201161UDI-DIDate15 Oct 2026RegisteredStatusActive EUDAMED: not on the EU market

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDR Active

Specification

EUDAMED

Device Name
Fully Automated Coagulation Analyzer
Model / Reference
SF-8050, SF-8100, SF-8100C, SF-8200, SF-8200C, SF-8300, SF-9200
Primary DI / UDI-DI
06957705201161
Basic UDI-DI
69577052FACAU8
EMDN Code
W0202020102 Automated coagulometers
Device Class
Class A

Manufacturer details

EUDAMED SRN
CN-MF-000028971
Authorised representative
MedNet EC-REP GmbH DE-AR-000000002

Properties

  • Professional Testing
  • Surgical Instrument

Other properties (9)

  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Reagent: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • New Device: No