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Angio Interventie Pack

EUDAMED

Class IIa (EU MDR)

Ref 103918AQRef 103918ANRef 103918AM

by Medica Europe B.V.

Identity

Trade Name: ANGIO INTERVENTIE PACK EUDAMED
Device Name: Custom Procedure Trays EUDAMED
Model / Reference: 103918AQ EUDAMED
103918AN EUDAMED
103918AM EUDAMED

Identifiers

Primary DI / UDI-DI: 08710685137794 EUDAMED
08710685115907 EUDAMED
08710685090242 EUDAMED
Basic UDI-DI: 8710685TF07001002RZ EUDAMED
EMDN Code: V0599 CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class: Class IIa EUDAMED
Medical Purpose: No EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

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

Angio Interventie Pack by Medica Europe B.V. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

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Also classified as Ophthalmic surgical procedure kit, non-medicated, single-use.

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Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer: Medica Europe B.V.
EUDAMED SRN: NL-PR-000000117

Sources (3)

EUDAMED 1c8409a5-52f9-4d7c-a45a-7151ba9f16d6 61 fields · synced Jul 25, 2026
EUDAMED 56b3abff-faac-4397-a26d-368e22333edd 61 fields · synced May 17, 2026
EUDAMED f30f7a8f-613a-445b-91f0-fd5673a2dbcf 61 fields · synced May 18, 2026