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Vitreoretinal Cannulae.

by Sterimedix Ltd 4 variants

Ref M4486-02/10Model M4474-02/10

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number50560304F11-FXQ Basic UDI-DI 25056030402924UDI-DIDate18 Mar 2025RegisteredStatusActive

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  • Withdrawn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
Vitreoretinal Cannulae.
Model / Reference
M4474-02/10, M4486-02/10
Primary DI / UDI-DI
25056030402924
Basic UDI-DI
50560304F11-FXQ
EMDN Code
Q021101 Occular irrigation and aspiration cannulas, single-use
Device Class
Class IIa
EU market of registration
France

Manufacturer details

EUDAMED SRN
GB-MF-000011604
Authorised representative
Bausch & Lomb GmbH DE-AR-000006810

Other devices from Sterimedix Ltd

See all devices from Sterimedix Ltd →

Properties

  • Sterile
  • Administering Medicine

Other properties (11)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No