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CI OMS FORMDEBFARM17310276SUSPECT ADVERSE REACTION REPORT I. REACTION INFORMATION 1. PATIENT INITIALS1a. COUNTRYDEprivacy2. DATE OF BIRTH DAMO2a. AGE3. SEXYR46 REACTION ONSET DAMOYRMale812 CHECK ALL
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What is de-bfarm-17310276?
de-bfarm-17310276 is a form required by the German Federal Institute for Drugs and Medical Devices (BFARM) for reporting information related to medical devices.
Who is required to file de-bfarm-17310276?
Manufacturers, importers, and distributors of medical devices are required to file de-bfarm-17310276.
How to fill out de-bfarm-17310276?
de-bfarm-17310276 can be filled out online on the BFARM website or manually using the provided form.
What is the purpose of de-bfarm-17310276?
The purpose of de-bfarm-17310276 is to ensure the safety and effectiveness of medical devices in the German market.
What information must be reported on de-bfarm-17310276?
Information such as device identification, technical documentation, risk assessment, and post-market surveillance data must be reported on de-bfarm-17310276.
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