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Phacoemulsification/ Vitrectomy System

by VitreQ B.V. 3 variants

Ref EQ00.R02

Phacoemulsification/ Vitrectomy System (EQ00.R02) is a Class IIb device made by Vitreq B.V., registered in EUDAMED on 19 May 2026 (Basic UDI-DI 871921422994GQ), active as of 24 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

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

Source EUDAMED, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number871921422994GQ Basic UDI-DI 08719214223649UDI-DIDate19 May 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Phacoemulsification/ Vitrectomy System
Model / reference
EQ00.R02
Primary DI / UDI-DI
08719214223649
Basic UDI-DI
871921422994GQ
Direct marketing DI
08719214223649
EMDN code
Z1212020702 Phaco-vitrectomy systems
Device class
Class IIb
System or procedure pack
System which is a device in itself
EU registration type
Standard device
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
NL-MF-000000424

Similar devices in this category

Other devices filed under PHACO-VITRECTOMY SYSTEMS.

Other devices from Vitreq B.V.

See all devices from Vitreq B.V. →

Properties

Other properties (14, all answered No)