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CUSA® Clarity

by Integra LifeSciences (Ireland) Limited 9 variants

Ref C7412KIT

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number038178B0002CSSZD Basic UDI-DI 10381780536208UDI-DIDate18 Sep 2026RegisteredStatusActive

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  • Withdrawn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
CUSA Clarity Ultrasonic Surgical Aspiration System Procedure Packs
Model / Reference
C7412KIT
Primary DI / UDI-DI
10381780536208
Basic UDI-DI
038178B0002CSSZD
EMDN Code
Z12010880 Instruments for ultrasonic surgery - hardware accessories
Device Class
Class III
Medical Purpose
For use in surgical procedures where fragmentation, emulsification and aspiration of soft and hard (e.g. bone) tissue is desirable.

Manufacturer details

EUDAMED SRN
IE-PR-000004000

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Properties

Other properties (1)

  • Sterile: No