EudaMed Scan vs Medical Device Directive Uso & Estadísticas

EudaMed Scan reads the human-readable text from a medical device label and searches the European Commission EUDAMED for that medical device. The UDI DI portion of the device label is used to search EUDAMED. Locate your code and click Search. EudaMed Scan requires an in-app purchase to read the human-readable text. App offers • Auto-renewable subscription with • 1 year ($8.49) • Your subscription will be charged to your Apple account at confirmation of purchase and will automatically renew (at the duration selected) unless auto-renew is turned off at least 24 hours before the end of the current period. • Current subscription may not be canceled during the active subscription period; however, you can manage your subscription and/or turn off auto-renewal by visiting your Apple Account Settings after purchase. • Privacy policy: https://eudamed.com/Eudamed%20Privacy%20Policy.pdf • Terms of Use: https://www.apple.com/legal/internet-services/itunes/dev/stdeula/
  • App Store de Apple
  • Gratis
  • Medicina

Clasificación de tiendas

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This app allows you to search text in a piece of legislation, the EU directives regarding active implantable medical devices, medical devices, and in vitro diagnostic medical devices, including the last technical revision brought about by Directive 2007/47/EC. VISAMED is not responsible for the correctness, completeness and application of the displayed texts and search results provided by this app. The app is provided as is, use at own risk.
  • App Store de Apple
  • Gratis
  • Medicina

Clasificación de tiendas

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EudaMed Scan frente a Medical Device Directive: comparación de la clasificación

Comparar la tendencia de clasificación de EudaMed Scan en los últimos 28 días con Medical Device Directive

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Comparación de las clasificaciones EudaMed Scan frente a Medical Device Directive por países

Comparar la tendencia de clasificación de EudaMed Scan en los últimos 28 días con Medical Device Directive

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Empieza ya
EudaMed Scan VS.
Medical Device Directive

enero 6, 2025