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Individo-Set

by Imtegra GmbH & Co KG 210 variants

Ref 1014 2201

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 Number4260253261014RP Basic UDI-DI 04260530128469UDI-DIDate24 Jan 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  • Withdrawn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
Individo-Set - I
Model / Reference
1014 2201
Primary DI / UDI-DI
04260530128469
Basic UDI-DI
4260253261014RP
EMDN Code
V0599 Clinical procedures kits not included in other classes - other
Device Class
Class I
Medical Purpose
zur Unterstützung einer medizinischen Behandlung

Manufacturer details

EUDAMED SRN
DE-PR-000006448

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Category: Ophthalmic surgical procedure kit, non-medicated, single-use

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Properties

  • Sterile