Statistics for QUIBIM

7Total Devices

4Basic UDI-DIs

0Not destined for EU market

0Certificates

0Valid

0Expiring < 6 months

1Countries

Certificate health for QUIBIM

No certificates registered for this manufacturer.

Showing 1–7 of 7 devices.

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
1.0	`1.0`	`08437021468045`	1	On the market
1.1	`1.1`	`08437021468113`	1	On the market
2.5	`2.5`	`08437021468229`	1	On the market
2.3	`2.3`	`08437021468151`	1	On the market
3.0	`3.0`	`08437021468250`	1	On the market
2.4	`2.4`	`08437021468182`	1	On the market
1.0	`1.0`	`08437021468090`	1	On the market

Devices placed in 1 country

MD Atlas update: May 27, 2026

ES-MF-000000668

Active

Address: Avenida Aragón, 30, 13th floor, Office J, 46021, Valencia (Spain), 30 46021 Valencia
Role: Manufacturer
Date of registration: Jan 14, 2021
Country: ES Spain

Address: 30, AVENIDA ARAGÓN, 30, 13TH FLOOR, OFFICE J, 46021, VALENCIA (SPAIN) 46021 VALENCIA SPAIN
Phone: +34 961243225
Email: contact@quibim.com
Website: www.quibim.com

MURILLO MATEO Erick
Among additional duties, the main responsibilities are the one mentioned on Article 15 of the EU MDR 2017/745: - Conformity of the product device to the Medical Device Regulation and Quality Management System - Conformity of the Technical Documentation and EU Declaration of conformity - Compliance with Post-Market Surveillance (PMS) following Article 10(10) - Compliance with the Vigilance Reporting obligations (Article 87 to 91)
Hidden