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DEPOIK09-03

by M.E.D. Medical Products GmbH

Ref DEPOIK09-03Model Katarakt

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 Number426006664-Kata-67 Basic UDI-DI 14251563622984UDI-DIDate24 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  • Withdrawn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

Model / Reference
Katarakt, DEPOIK09-03
Primary DI / UDI-DI
14251563622984
Basic UDI-DI
426006664-Kata-67
EMDN Code
Q021199 Ophthalmic surgery instruments, single-use - other
Device Class
Class I
Medical Purpose
Kundenindividuelle Zusammenstellung verschiedener CE-gekennzeichneter Einweg-Medizinprodukte, die für einen speziellen Eingriff im OP benötigt werden, steril in einer einzigen Verpackung. Ein individuell zusammengestelltes OP-Set ist nicht für verschiedene Anwender gedacht.

Manufacturer details

EUDAMED SRN
DE-PR-000019570

Other devices from M.E.D. Medical Products GmbH

See all devices from M.E.D. Medical Products GmbH →

Properties

  • Sterile