Rivarp Medical Pvt.ltd.,

Aucun certificat enregistré pour ce fabricant.

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  N.R sushma

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• N.R sushma
  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. the technical documentation and the EU declaration of conformity are drawn up and kept up to date. the post-market surveillance obligations are complied with in accordance with Article 10(10). in the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV is issued.
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Aucun dispositif enregistré pour ce fabricant.

• Malta Medicines Authority
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• N.R sushma — Rivarp