Skip to content

Pipette Tip

by Jiangsu Kahotest Citotest Labware Manufacturing Co., Ltd 2 variants

Ref 16955257400039Model 10ul/200ul/300ul/1000ul/5ml/10ml

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number69552574PT001SP Basic UDI-DI 16955257400039UDI-DIDate10 May 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  • Withdrawn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/IVDR Active

Specification

EUDAMED

Device Name
Pipette Tip
Model / Reference
10ul/200ul/300ul/1000ul/5ml/10ml, 16955257400039
Primary DI / UDI-DI
16955257400039
Basic UDI-DI
69552574PT001SP
EMDN Code
W05019001, W0599
Device Class
Class A
EU market of registration
Greece

Manufacturer details

EUDAMED SRN
CN-MF-000034323
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Jiangsu Kahotest Citotest Labware Manufacturing Co., Ltd

See all devices from Jiangsu Kahotest Citotest Labware Manufacturing Co., Ltd →

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