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Pipette Tips

by Shandong Chengwu Medical Products Factory 17 variants

Ref MLA:1000ulModel Gilson：10ul、200ul、1000ul、5000ul、10000ul Eppendorf：10ul、200ul、300ul、1000ul、10000ul Oxford：200ul、1000ul MLA：200ul、1000ul Qiujing：4*49、4#、500ul Dalong：5ml

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number697390596PT01RU Basic UDI-DI 06973905962633UDI-DIDate19 Oct 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  • Withdrawn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 Tips
Model / Reference
Gilson：10ul、200ul、1000ul、5000ul、10000ul Eppendorf：10ul、200ul、300ul、1000ul、10000ul Oxford：200ul、1000ul MLA：200ul、1000ul Qiujing：4*49、4#、500ul Dalong：5ml, MLA:1000ul
Primary DI / UDI-DI
06973905962633
Basic UDI-DI
697390596PT01RU
EMDN Code
W0599 IVD general use consumable devices - other
Device Class
Class A
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
CN-MF-000003370
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Shandong Chengwu Medical Products Factory

See all devices from Shandong Chengwu Medical Products Factory →

Properties

Other properties (11)

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