Italian Medical Device Registration

Medes Inc – USA: FDA Designated Agent – Arazy Group

NSIS REGISTRATION – ITALY
Medical devices of all classes, active implantable medical devices, and procedure packs and kits sold in Italy must be registered in an Italian database ("Repertorio") administered by the Ministry of Health through its new system, NSIS. This requirement is a national regulation with no relation to the fact that the product might already be CE marked. Medes Limited is qualified and experienced in this registration and will carry out for your company all the activities required to complete the process.

If you want to know more about regulatory issues of Medical Devices, click here.

Medes Limited – EU: CE Authorized Representative – Arazy Group

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	Contact us

Need more information? Do you have any specific question? Would like to get a quote? Here are 4 easy options:

	Phone us to our call centers: English: +4420.8123.8056 GMT UK - London, UK Español: +5411.4723.9147 EST USA - Buenos Aires, AR

	Skype us: English: betarazy Español: medes.argentina

	E-Mail us: CE@medeseurope.co.uk

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