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CartRevive

by Hy2Care BV

Ref 111-02-100Model CartRevive instrument set 1.1 EU

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 Number87208927365119N Basic UDI-DI 87208927365120UDI-DIDate21 Apr 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  • Withdrawn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
CartRevive instrument set
Model / Reference
CartRevive instrument set 1.1 EU, 111-02-100
Primary DI / UDI-DI
87208927365120
Basic UDI-DI
87208927365119N
EMDN Code
V901699 Specialist surgical instruments and kits not included in other classes, single-use - other
Device Class
Class IIb
Medical Purpose
The CartRevive instrument set is a combination of sterile CE marked components used for applying CartRevive hydrogel implant on to a cartilage defect. Only meant to be used in combination with CartRevive hydrogel implant.

Manufacturer details

EUDAMED SRN
NL-PR-000053479

Properties

  • Sterile