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Edpo-10D-02

by Yelatma Instrument-Making Enterprise Joint-Stock Company

Ref 1014865

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4602122004971NU Basic UDI-DI 04602122002847UDI-DIDate17 Mar 2022RegisteredStatusActive

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  • Withdrawn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

Device Name
Edpo
Model / Reference
1014865
Primary DI / UDI-DI
04602122002847
Basic UDI-DI
4602122004971NU
Direct Marketing DI
04602122002847
EMDN Code
Z12011399 Cleaning, disinfection and sterilisation instruments - other
Device Class
Class I
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
RU-MF-000008411
Authorised representative
QbD RepS BV BE-AR-000000040

Other devices from Yelatma Instrument-Making Enterprise Joint-Stock Company

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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