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SL 25i- LED

by Labo America Inc.

Ref 8127701Model Slit lamp SL20i,SL25i,SLx 40,SLx45,eVO300,eVO350,eVO400,eVO450

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 Number81017855SLITLAMPAT Basic UDI-DI 00810178550340UDI-DIDate23 Sep 2024RegisteredStatusActive

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  • Withdrawn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
Slit Lamp
Model / Reference
Slit lamp SL20i, SL25i, SLx 40, SLx45, eVO300, eVO350, eVO400, eVO450, 8127701
Primary DI / UDI-DI
00810178550340
Basic UDI-DI
81017855SLITLAMPAT
Direct Marketing DI
00810178550340
EMDN Code
Z12120108 Slit lamps
Device Class
Class I
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
US-MF-000044352
Authorised representative
Labomed Europe b.v. NL-AR-000022889

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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