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Liver Function Analysis Meter

by Hangzhou Lysun Biotechnology Co., Ltd

Ref LMF-101, 3993600101

Active European Union

CE IVDR CE IVDD

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD Number69717712002007Q Basic UDI-DI Date21 Nov 2023RegisteredStatusActive
European UnionCE/IVDR Number69717712002007Q Basic UDI-DI Date21 Nov 2023RegisteredStatusActive

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  • Withdrawn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/IVDD, CE/IVDR Active

Specification

EUDAMED

Model / Reference
LMF-101, 3993600101
Primary DI / UDI-DI
06971771200200, D-69717712002007Q
Basic UDI-DI
69717712002007Q, B-69717712002007Q
EMDN Code
W0201069099, W02020680
Device Class
Class A
Class IVD General
EU market of registration
Netherlands
Germany

Manufacturer details

EUDAMED SRN
CN-MF-000010254
Authorised representative
Lotus NL B.V. NL-AR-000000121

Other devices from Hangzhou Lysun Biotechnology Co., Ltd

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Properties

  • Near-Patient Testing
  • Professional Testing
  • Companion Diagnostics
  • Surgical Instrument

Other properties (7)

  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Reagent: No
  • Self Testing: No
  • New Device: No