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Katarakt-Set

by biocon Medizintechnik GmbH 130 variants

Ref 92203682

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 Number42514803010K8 Basic UDI-DI 04251480313432UDI-DIDate31 Jul 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  • Withdrawn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
OP-Set
Model / Reference
92203682
Primary DI / UDI-DI
04251480313432
Basic UDI-DI
42514803010K8
EMDN Code
V901699 Specialist surgical instruments and kits not included in other classes, single-use - other
Device Class
Class IIa
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-000019552

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Properties

  • Sterile