Skip to content

High Q Cell All in One Duo

by Zuccato HC Srl

Ref HIGH Q CELL ALL IN ONE DUO

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number805168729HQCLQDIU5 Basic UDI-DI 08051687290163UDI-DIDate20 Jul 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  • Withdrawn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
High Q Cell All in One Liquid
Model / Reference
HIGH Q CELL ALL IN ONE DUO
Primary DI / UDI-DI
08051687290163
Basic UDI-DI
805168729HQCLQDIU5
EMDN Code
A99 Devices for administration, withdrawal and collection - other
Device Class
Class IIa
Medical Purpose
kit PRP per medicina rigenerativa

Manufacturer details

EUDAMED SRN
IT-PR-000054479

Other devices from Zuccato HC Srl

See all devices from Zuccato HC Srl →

Properties

  • Sterile