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CO-RE II Tips, black, sterile

by Hamilton Bonaduz AG 6 variants

Ref 235935

Active European Union

CE IVDR CE IVDD

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR NumberB-07630032623859 Basic UDI-DI 07630032623859UDI-DIDate17 May 2022RegisteredStatusActive
European UnionCE/IVDD NumberB-07630032623859 Basic UDI-DI 07630032623859UDI-DIDate17 May 2022RegisteredStatusActive

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  • Withdrawn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/IVDR, CE/IVDD Active

Specification

EUDAMED

Device Name
Low Vol. Co.re Tips, Sterile
Low Vol. Co-Re Tips, Sterile
Model / Reference
235935
Primary DI / UDI-DI
07630032623859
Basic UDI-DI
B-07630032623859, 76300326235935LL
EMDN Code
W0503020202 Pipettes, tips without filter
Device Class
Class IVD General
Class A
EU market of registration
Germany
Austria

Manufacturer details

EUDAMED SRN
CH-MF-000013585
Authorised representative
Johner Medical GmbH DE-AR-000011832

Other devices from Hamilton Bonaduz AG

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Properties

  • Sterile

Other properties (10)

  • 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