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SL200

by Zumax Medical CO., LTD.

Ref 843800011000-00

SL200 (843800011000-00) is a Class I device made by Zumax Medical Co., LTD, registered in EUDAMED on 8 Oct 2026 (Basic UDI-DI 69450955Slitlamp7R), active as of 7 Nov 2026.

Active European Union

CE MDR

Valid until

No date given

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

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number69450955Slitlamp7R Basic UDI-DI 06945095556183UDI-DIDate8 Oct 2026RegisteredStatusActive

Official records

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  • Withdrawn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
843800011000-00
Primary DI / UDI-DI
06945095556183
Basic UDI-DI
69450955Slitlamp7R
EMDN code
Z12120108 Slit lamps
Device class
Class I
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
CN-MF-000011126
Authorised representative
MedNet EC-REP GmbH DE-AR-000000002

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Properties

Other properties (14, all answered No)