Skip to content

Real-time Quantitative Thermal Cycler

by Suzhou Molarray Co., Ltd 7 variants

Ref MAtrix-6Model MA-6000,P30,MA-3200Q,MA-5000,MA-6000P,MA-9600P,MAtrix-6,MAtrix-4

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number697527577001NV Basic UDI-DI 06975275770092UDI-DIDate30 Apr 2026RegisteredStatusActive

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  • Withdrawn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

Model / Reference
MA-6000, P30, MA-3200Q, MA-5000, MA-6000P, MA-9600P, MAtrix-6, MAtrix-4
Primary DI / UDI-DI
06975275770092
Basic UDI-DI
697527577001NV
Direct Marketing DI
06975275770092
EMDN Code
W02050116 Nucleic acid testing integrated extraction /amplification /detection systems
Device Class
Class A
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
CN-MF-000053786
Authorised representative
Caretechion GmbH DE-AR-000005946

Other devices from Suzhou Molarray Co., Ltd

See all devices from Suzhou Molarray Co., Ltd →

Properties

  • Professional Testing
  • Surgical Instrument

Other properties (9)

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