Statistics for NBE

7Total Devices

7Basic UDI-DIs

0Not destined for EU market

0Certificates

0Valid

0Expiring < 6 months

2Countries

Certificate health for NBE

No certificates registered for this manufacturer.

Showing 1–7 of 7 devices.

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
RPE00	`RPE00`	`19349285000977`	1	On the market
Accusol	`RPE04`	`19349285000991`	1	On the market
RPE02	`RPE02`	`19349285000984`	1	On the market
HF19	`HF19`	`19349285000274`	1	On the market
HF12	`HF12`	`19349285000267`	1	On the market
HF07+	`HF07+`	`19349285000250`	1	On the market
HF03	`HF03`	`19349285000243`	1	On the market

Devices placed in 2 countries

EUDAMED update: Nov 28, 2025

BE-MF-000003701

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

HERMANS Anik
- Post-market surveillance obligations in accordance with Article 10(10); - Reporting obligations referred to in Articles 87 to 91 - Conformity of the devices in accordance with the quality management system under which the devices are manufactured, before a device is released
Hidden
DUROWOJU Damilola
- Reporting obligations referred to in Articles 87 to 91 (back-up for Anik Hermans)
Hidden
LEIJNEN Veerle
- Technical Documentation and EU declaration of conformity for Accusol and Aquamax products
Hidden
STAMPELLA Alessandra
- Conformity of the devices in accordance with the quality management system under which the devices are manufactured, before a device is released (back-up for Anik Hermans)
Hidden