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P111F012 Client QuestionnaireApplicant (precise legal form of company name) This form serves as the basis for the offer and consists of two Parts: Part A requires general information about the company,
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Read the client-questionnaire carefully to understand the information required.
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Who needs client-questionnaire-mdr-tuev-nord?

01
Companies seeking MDR certification from TUV Nord.
02
Organizations looking to ensure compliance with medical device regulations.
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It is a questionnaire used by TÜV NORD for clients to report information related to medical devices under the Medical Device Regulation (MDR).
Manufacturers, importers, and distributors of medical devices are required to file the client-questionnaire-mdr-tuev-nord.
The client-questionnaire-mdr-tuev-nord can be filled out online on the TÜV NORD website or through a physical form provided by TÜV NORD.
The purpose of the client-questionnaire-mdr-tuev-nord is to gather information about medical devices to ensure compliance with the Medical Device Regulation.
Information such as device classification, technical documentation, conformity assessment, post-market surveillance, and unique device identification must be reported on the client-questionnaire-mdr-tuev-nord.
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