PubMed-Literatur
Publikationen zu Medizinprodukten aus PubMed / NCBI
Analyse der Trends bei FDA-zurückgerufenen Hüftgelenksersatzgeräten: Eine retrospektive Überprüfung.
Mehr lesen →Cybersecurity breaches in medical devices: analyzing FDA safety communications in response to patient security concerns.
Mehr lesen →Ein mehrdimensionales Indexrahmenwerk zur Bewertung der regulatorischen Anwendbarkeit von ISO 10328 unter Verwendung eines Fallstudie eines Prothesen-Knie
Mehr lesen →Urologic Device Innovation and Trends: An Analysis of Food and Drug Administration Approvals From 1990 to 2023.
Mehr lesen →Medical Device Regulation - Who Does the FDA Serve?
Mehr lesen →Device failures and patient adverse events from EUS: 26-year FDA MAUDE analysis (2000-2025).
Mehr lesen →Artificial intelligence as medical device in radiology in 2025: the regulatory scenario in the EU, USA, and China.
Mehr lesen →Clinical Trial Design and Regulatory Requirements for Artificial Intelligence as a Medical Device: A PRISMA-ScR-Guided Scoping Review of Global Guidance and Evidence (2017-2025).
Mehr lesen →The history of state preemption and medical device regulation: lessons for artificial intelligence oversight.
Mehr lesen →FDA-Regulated AI-Enabled Medical Devices With Pediatric Indications.
Mehr lesen →Use and regulation of patient-specific three-dimensional printing in medicine: a survey of physician end-users.
Mehr lesen →Keine passenden Artikel.
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