Skip to content

Biopsy Pipette

by ICSION Medical Pty Ltd 49 variants

Ref B-23-25

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

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/MDR Number93593510MicropipetteM6 Basic UDI-DI 09359351000735UDI-DIDate19 Jan 2023RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Micromanipulation Pipettes
Model / Reference
B-23-25
Primary DI / UDI-DI
09359351000735
Basic UDI-DI
93593510MicropipetteM6
EMDN Code
U0802030101 Biopsy pipettes for assisted reproduction
Device Class
Class I
EU market of registration
Bulgaria

Manufacturer details

EUDAMED SRN
AU-MF-000030208
Authorised representative
Compliance Management Solutions Europe LTD BG-AR-000020809

Other devices from ICSION Medical Pty Ltd

See all devices from ICSION Medical Pty Ltd →

Properties

  • Sterile

Other properties (12)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No