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KMSISDEL01 SET, DELIVERY, instruments

by Spanish Kits Company S.L.

Ref 1-08227

Active European Union

CE MDR

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/MDR Number84305131000INSTLD Basic UDI-DI 18430513062476UDI-DIDate21 Oct 2026RegisteredStatusActive

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  • Withdrawn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/MDR Active

Specification

EUDAMED

Model / Reference
1-08227
Primary DI / UDI-DI
18430513062476
Basic UDI-DI
84305131000INSTLD
EMDN Code
Z129099 Various instruments for functional exploration and therapeutic interventions - other
Device Class
Class I
Medical Purpose
Proporcionar productos sanitarios y el soporte para dejar los mismos, denominado, campo quirúrgico, para la realización de procesos médico-quirúrgicos.

Manufacturer details

EUDAMED SRN
ES-PR-000014340

Properties

Other properties (1)

  • Sterile: No