The Seller has implemented a material vigilance procedure for medical devices in accordance with legal requirements.
The Client agrees to communicate to the Seller, WITHOUT DELAY, any incident and risk of incident of which he might be aware concerning a medical device delivered by the Seller. If the Client reports the incident or risk of incident, he will also inform the Seller WITHOUT DELAY. The Client agrees to collect and communicate to the Seller all the information requested by the latter concerning the incident or risk of incident.
If the Seller identifies an incident or risk of incident concerning a medical device delivered to the Client, he agrees to inform the Client as soon as possible. The Client agrees to collect and communicate to the Seller all the information requested by the latter concerning the incident or risk of incident.
If the Seller informs the Client of a withdrawal or recall measure, the Client agrees to :
In the event of withdrawal or recall of the products, the Client first agrees to store the affected products until recovery or destruction order by the Seller.
If the Seller requests the recovery of products subject to withdrawal or recall, the transport will be, at the Seller's choice:
If the Seller requests the recovery of products subject to withdrawal or recall, the destruction will be, at the Seller's choice:
The products subject to recovery or destruction may, at the Seller's choice:
THE ADHERENCE TO THESE RULES IS AN ESSENTIAL CONDITION FOR THE SELLER. IN THE EVENT OF NON-COMPLIANCE WITH THESE REQUIREMENTS BY THE CLIENT, THE SELLER RESERVES THE RIGHT TO REFUSE ANY FURTHER ORDERS.
For more than 15 years, Identités has been offering solutions to improve the comfort and independence of the elderly and disabled.
This item has been added to your cart