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Jinquan

by Guangdong Jinquan Medical Technology Co., Ltd. 14 variants

Model JQ-GM620 JQ-GM630 JQ-GM640

Active European Union

CE IVDR

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/IVDR Number697534035JINQUANPSCLSZ Basic UDI-DI 16975340350027UDI-DIDate19 Sep 2022RegisteredStatusActive

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  • Withdrawn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/IVDR Active

Specification

EUDAMED

Device Name
Laser Slide Printer
Model / Reference
JQ-GM620 JQ-GM630 JQ-GM640
Primary DI / UDI-DI
16975340350027
Basic UDI-DI
697534035JINQUANPSCLSZ
EMDN Code
W02069099 Various sample processing instruments - other
Device Class
Class A
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
CN-MF-000023901
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Guangdong Jinquan Medical Technology Co., Ltd.

See all devices from Guangdong Jinquan Medical Technology Co., Ltd. →

Properties

  • Professional Testing
  • Companion Diagnostics
  • Surgical Instrument

Other properties (8)

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