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Solatronic SL-3

by Elektronika i Elektromedycyna M.Lewandowski Sp.J.

Ref Solatronic SL-3

Active European Union

CE MDR

Valid until

16 Jan 2030

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier TUV NORD Polska Sp. z o.o

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberTNP/MDR/0030/2034/2025 Date23 Sep 2026IssuedStatusActive expires 16 Jan 2030

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • TNP/MDR/0030/2034/2025 Active Supplemented

    Quality management system EU MDR

    Certifier
    TUV NORD Polska Sp. z o.o 2274
    Issued
    23 Sep 2026
    Expires
    16 Jan 2030
    Reason
    Other

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
Solatronic SL-3
Primary DI / UDI-DI
05906660092032
Basic UDI-DI
5906660092SL3CS
Direct Marketing DI
05906660092032
EMDN Code
Z120615 Therapeutic lasers
Device Class
Class IIa
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
PL-MF-000032400

Other devices from Elektronika i Elektromedycyna M.Lewandowski Sp.J.

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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