Statistics for Euromi Biosciences

518Total Devices

518Basic UDI-DIs

0Not destined for EU market

0Certificates

0Valid

0Expiring < 6 months

2Countries

Certificate health for Euromi Biosciences

No certificates registered for this manufacturer.

No devices registered for this manufacturer.

Devices placed in 2 countries

MD Atlas update: May 27, 2026

BE-MF-000020089

Active

Name: Federaal Agentschap voor Geneesmiddelen en Gezondheidsproducten/ Afdeling Gezondheidsproducten
SRN: BE-CA-007
Phone: +32 2 528 40 00
Email: notifications.meddev@fagg-afmps.be

MASCREZ Olivia
- ensure that the conformity of the devices is appropriately checked, in accordance with the QMS under which the devices are manufactured, before release; -ensure that the technical documentation & EU DOC are drawn up & kept up-to-date - ensure that the PMS obligations are complied with in accordance with the regulatory framework in place; - ensure that the reporting obligations are fulfilled - Ensure that for investigational devices, the Annex XV, Chap II Sec 4.1 statement is issued
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BENOIT Perrine
- ensuring that the conformity of the devices is appropriately checked, in accordance with the quality management system under which the devices are manufactured, before a device is released; -ensuring that the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date
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