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Aicor

by Zhejiang Aicor Medical Technology Co., Ltd. 3 variants

Ref C01Model Petri Dish, Culture Plate, Culture Flask

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 Number697092794CULTURE0016Z Basic UDI-DI 06970927944012UDI-DIDate25 May 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  • Withdrawn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

Device Name
Culture Equipment Consumables (Petri Dish, Culture Plate, Culture Flask)
Model / Reference
Petri Dish, Culture Plate, Culture Flask, C01
Primary DI / UDI-DI
06970927944012
Basic UDI-DI
697092794CULTURE0016Z
EMDN Code
W0599 IVD general use consumable devices - other
Device Class
Class A
EU market of registration
Portugal

Manufacturer details

EUDAMED SRN
CN-MF-000040036
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Zhejiang Aicor Medical Technology Co., Ltd.

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Properties

  • Professional Testing

Other properties (10)

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