Bfarm recall database. On the following pages, the BfArM provides links to laws and ord...

Bfarm recall database. On the following pages, the BfArM provides links to laws and ordinances relating to medical device law and to other competent authorities. The Federal Institute for Drugs and Medical Devices (BfArM) is authorized to disclose non-public information to the United States Food and Drug Administration (FDA) regarding BfArM-regulated Das Bundesinstitut für Arzneimittel und Medizinprodukte (BfArM) ist eine selbstständige Bundesoberbehörde im Geschäftsbereich des Bundesministeriums für Gesundheit. The Federal Institute for Drugs and Medical Devices (Bundesinstitut für Arzneimittel und Medizinprodukte, BfArM) is an independent federal higher authority within the portfolio of the Federal Ministry of Health. In addition, information on the tasks of the BfArM is listed and the process for placing medical devices on the market is explained. Federal Institute for Drugs and Medical Devices (BfArM) Better health for all citizens is the goal of the work of the Federal Centre for Health Education. The Federal Institute for Drugs and Medical Devices (Bundesinstitut für Arzneimittel und Medizinprodukte, BfArM) is an independent federal higher authority within the portfolio of the Federal Ministry of Health. The Federal Institute for Drugs and Medical Devices (German: Bundesinstitut für Arzneimittel und Medizinprodukte – BfArM) is the medical regulatory body in Germany. . Jul 15, 2025 · The Federal Institute for Drugs and Medical Devices (BfArM) is an independent federal higher authority within the portfolio of the Federal Ministry of Health (BMG) with the responsibility to ensure the safety of medicinal products and patients in Germany. ltymx jkbp nvlkxj oet qclyhr dscef lqefe dweri gzej jnpawtg