Statistics for GreenBone Ortho Spa

83Total Devices

1Basic UDI-DIs

0Not destined for EU market

1Certificates

1Valid

0Expiring < 6 months

1Countries

Certificate health for GreenBone Ortho Spa

Showing 76–83 of 83 devices.

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
HC100060PS	`HC100060PS`	`08053848341301`	1	On the market
HC100030PS	`HC100030PS`	`08053848341271`	1	On the market
GR102015PS	`GR102015PS`	`08053848340526`	1	On the market
GR051010PS	`GR051010PS`	`08053848340472`	1	On the market
GR204010PS	`GR204010PS`	`08053848340496`	1	On the market
GR407105PS	`GR407105PS`	`08053848341264`	1	On the market
HC100040PS	`HC100040PS`	`08053848341288`	1	On the market
GR407115PS	`GR407115PS`	`08053848340878`	1	On the market

Devices placed in 1 country

MD Atlas update: May 27, 2026

IT-MF-000033034

Active

Name: Ministero della salute - Direzione generale dei dispositivi medici e del servizio farmaceutico
SRN: IT-CA-070
Phone: +39 06 5994 3199/ +39 06 5994 3207
Email: segr.dgfdm@sanita.it

BONOMI Vanessa
1) the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date; 2) the post-market surveillance obligations (PMS Plan, PSUR) are complied with in accordance with Article 10(10) 3) to ensure the vigilance reporting obligations referred to in Articles 87 to 91 are fulfilled
Hidden
CHA Andrea
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;
Hidden
SALVAGNO Susanna
1) the technical documentation (CEP, CER, SSCP) is drawn up and kept up-to-date; 2) the post-market surveillance obligations (PMCF) are complied with in accordance with Article 10(10) 3) to ensure in the case of devices for performance studies intended to be used in the context of interventional clinical performance studies or other performance studies involving risks for the subjects, the statement referred to in Section 4.1 of Chapter II of Annex XV is issued.
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