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Clinnova Therapy Drop-End

by SEERS Medical Ltd EUDAMED

Active European Union

Ref NV3556Model Many

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number50561238CLNOVAFF Basic UDI-DIDate13 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates

0 certificates · EUDAMED

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

Specification

EUDAMED

Device Name
Clinnova
Model / Reference
Many, NV3556
Primary DI / UDI-DI
05056123840097
Basic UDI-DI
50561238CLNOVAFF
Direct Marketing DI
05056123840097
EMDN Code
V080202 Manual medical chairs
Device Class
Class I
Market of Registration
Malta

Manufacturer details

EUDAMED SRN
GB-MF-000003831
Authorised representative
Advena Limited MT-AR-000000234

Other devices from SEERS Medical Ltd

See all devices from SEERS Medical Ltd →

Properties

Other properties (13)

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