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Medilight

by Medicop - specialna oprema d.o.o.

Ref Instruction_manual_BHU_Medilight_Medintensive v2.4 ENModel Bead Head Unit

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 linked in EUDAMED

A group certificate may exist

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 Number3838578EQUSPEBHU788192P7Z Basic UDI-DIDate14 May 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
Bead Head Unit, Instruction_manual_BHU_Medilight_Medintensive v2.4 EN
Primary DI / UDI-DI
93838578000715
Basic UDI-DI
3838578EQUSPEBHU788192P7Z
Direct Marketing DI
93838578000715
EMDN Code
Z120309 Medical/medicinal gas pipeline systems and related accessories
Device Class
Class IIa
Market of Registration
Slovenia

Manufacturer details

EUDAMED SRN
SI-MF-000002144

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Properties

  • Implantable
  • Administering Medicine
  • Measuring Function

Other properties (10)

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