Statistics for Millet Innovation

73Total Devices

18Basic UDI-DIs

0Not destined for EU market

0Certificates

0Valid

0Expiring < 6 months

9Countries

Certificate health for Millet Innovation

No certificates registered for this manufacturer.

Showing 26–50 of 73 devices.

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
Coussinets Plantaires	`CC2613`	`03660396000021`	1	On the market
Coussinets Plantaires	`CC2612BE`	`03660396003633`	1	On the market
Coussinets Plantaires	`CC2614BE`	`03660396003657`	1	On the market
CD2613IT	`CD2613IT`	`03660396003190`	1	On the market
CD2611IT	`CD2611IT`	`03660396003176`	1	On the market
CD2612IT	`CD2612IT`	`03660396003183`	1	On the market
CC2613IT	`CC2613IT`	`03660396002650`	1	On the market
CC2614IT	`CC2614IT`	`03660396002667`	1	On the market
Digitubes®	`0221`	`03660396001684`	2	On the market
Doigtiers	`0361`	`03660396001974`	2	On the market
Doigtiers ajustables	`0350`	`03660396001318`	2	On the market
NORCC3	`NORCC3`	`08435232330786`	1	On the market
NORCC2	`NORCC2`	`08435232330816`	1	On the market
NORCC1	`NORCC1`	`08435232330823`	1	On the market
CC2614AL	`CC2614AL`	`03660396004043`	1	On the market
CC2613AL	`CC2613AL`	`03660396004036`	1	On the market
CD1FI	`CD1FI`	`03660396015988`	1	On the market
CD3FI	`CD3FI`	`03660396016008`	1	On the market
CD2FI	`CD2FI`	`03660396015995`	1	On the market
CD2612NL	`CD2612NL`	`03660396009338`	1	On the market
CD2613NL	`CD2613NL`	`03660396009345`	1	On the market
CD2611NL	`CD2611NL`	`03660396009321`	1	On the market
Orthèse corrective souple de jour Hallux Valgus "oignon"	`0521`	`03660396005200`	1	On the market
Orthèse Poignet Pouce EPITACT SPORT	`G481G`	`03660396021811`	1	On the market
Orthèse Poignet Pouce EPITACT SPORT	`G482D`	`03660396021828`	1	On the market

Devices placed in 9 countries

EUDAMED update: Nov 7, 2024

FR-MF-000004611

Active

AUBRY Myriam
- The conformity of the devices, in accordance with the quality management system under which the devices are manufactured, before a device is released; - The technical documentation and the EU declaration of conformity, - The post-market surveillance obligations complied with in accordance with Article 10(10); - The reporting obligations referred to in Articles 87 to 91; - Clinical investigations in line with the statement referred to in Section 4.1 of Chapter II of Annex XV.
Hidden
LOPEZ Isabelle
- The conformity of the devices, in accordance with the quality management system under which the devices are manufactured, before a device is released; - The technical documentation and the EU declaration of conformity, - The post-market surveillance obligations complied with in accordance with Article 10(10); - The reporting obligations referred to in Articles 87 to 91; - Clinical investigations in line with the statement referred to in Section 4.1 of Chapter II of Annex XV.
Hidden