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513-T44L-Pu-T44-Q99

by Mjartan, s. r. o. 7 variants

Ref 513-T44L-PU-T44-Q99-39

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 Number8584196ortomedpooL6 Basic UDI-DI 08584196007200UDI-DIDate15 May 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  • Withdrawn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

Device Name
ortomed pooperačná a obväzová obuv
Model / Reference
513-T44L-PU-T44-Q99-39
Primary DI / UDI-DI
08584196007200
Basic UDI-DI
8584196ortomedpooL6
EMDN Code
Y063303 Ready-made orthotic shoes
Device Class
Class I
EU market of registration
Slovakia

Manufacturer details

EUDAMED SRN
SK-MF-000051525

Other devices from Mjartan, s. r. o.

See all devices from Mjartan, s. r. o. →

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