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Botexplantatie Fase a

by Medica Europe B.V. 5 variants

Ref 104740AJ

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, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8710685TF07001001RX Basic UDI-DI 08710685115495UDI-DIDate5 Dec 2022RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Custom Procedure Trays
Model / Reference
104740AJ
Primary DI / UDI-DI
08710685115495
Basic UDI-DI
8710685TF07001001RX
EMDN Code
V0599 Clinical procedures kits not included in other classes - other
Device Class
Class I
Medical Purpose
Custom procedure trays provide ready-to-use (medical) devices, to be used during surgical procedures or other medical interventions as intended by their legal manufacturer.

Manufacturer details

EUDAMED SRN
NL-PR-000000117

Related devices

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

Other devices from Medica Europe B.V.

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Properties

Other properties (1)

  • Sterile: No