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Custom Procedure Trays - EUDAMED Registration 08710685128938

Access comprehensive regulatory information for Custom Procedure Trays in the European Union medical device market through Pure Global AI's free database. This Class IIb device is registered with EU EUDAMED under Primary DI 08710685128938 and manufactured by Medica Europe B.V. in Netherlands.

This page provides complete registration details including trade name (CRISTA PUNCTIE), manufacturer information, competent authority (Ministerie van Volksgezondheid, Welzijn en Sport), and regulatory compliance data from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry, helping global MedTech companies navigate EU MDR regulations efficiently.

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EUDAMED Official Data
Class IIb
08710685128938
No
Custom Procedure Trays
Trade Name: CRISTA PUNCTIE
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Device Description (EMDN)

CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER

Device Classification
Risk Class
Class IIb
CND Nomenclatures Code
V0599
Trade Name
CRISTA PUNCTIE
Implantable
No
Reusable
No
Measuring Function
No
Registration Information
Primary DI
08710685128938
Basic UDI
8710685TF07001003S3
Active Status
No
Manufacturer
Manufacturer Name
Medica Europe B.V.
Country
Netherlands
Country Type
EU_MEMBER_STATE
Address
20 Galliërsweg Oss
Email
qa@medica-europe.nl
Regulatory Information
Competent Authority
Ministerie van Volksgezondheid, Welzijn en Sport
Applicable Legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Device Characteristics
Human Tissues
No
Animal Tissues
No