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ECLIPSIUM Polymer

by Tissium S.A.

Ref SM00166

Active European Union

CE MDR

Valid until

22 Sep 2031

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier TÜV SÜD Product Service GmbH

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberG70 104062 0008 Date23 Sep 2026IssuedStatusActive expires 22 Sep 2031

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
ECLIPSIUM Polymer
Model / Reference
SM00166
Primary DI / UDI-DI
03760279380575
Basic UDI-DI
376027938SM00185BL
Direct Marketing DI
03760279380575
EMDN Code
V9099 Various devices not included in other classes - other
Device Class
Class III
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
FR-MF-000050331

Other devices from Tissium S.A.

Properties

  • Sterile
  • Implantable
  • CMR Substance

Other properties (10)

  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No