Dispositivos médicos
Manténgase a la vanguardia con actualizaciones críticas e información sobre dispositivos médicos, sus regulaciones, estándares de la industria y estrategias de cumplimiento.
Dispositivos médicos
Manténgase a la vanguardia con actualizaciones críticas e información sobre dispositivos médicos, sus regulaciones, estándares de la industria y estrategias de cumplimiento.
Latest Dispositivos médicos Compliance Articles
A medida que las compras en línea se vuelven más comunes para las empresas, los beneficios de comprar en su moneda local son innegables.
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Explore las distinciones cruciales entre un dispositivo médico de Clase I, Clase II y Clase III mientras comprende sus características y matices regulatorios.
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Conozca la diferencia entre la autorización de la FDA y la aprobación de la FDA y cómo se aplican a los dispositivos y fármacos médicos.
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Su guía concisa para comprender y responder a un Aviso de acción de la FDA. Explorar tipos, estrategias y cómo crear planes de acción correctiva efectivos.
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Dispositivos médicos Regulations FAQ
For Medical Device Establishments, who must register?
Owners or operators of establishments involved in producing and distributing medical devices intended for the U.S. market must register annually with FDA and pay an annual registration fee.
What information is submitted for medical device establishment registration?
In addition to registering with FDA, most owners or operators of medical device establishments must also submit a list of all devices during their annual registration renewal.
- U.S. Facilities
- Initial importers must identify the manufacturers of the devices they are importing.
- A device must be listed if they fall under the any of the following:
- Contract Manufacturer
- Contract Sterilizer
- Manufacturer
- Relabeler / Repackager
- Remanufacturer
- Reprocessor of Single Use Device
- Specification Developer
- U. S. manufacturer of export only devices
- Non-U.S. Facilities
- Must list devices, provide a U.S. Agent, and identify importers.
Who must provide medical device listings?
In most cases, all medical device establishments required to register with FDA must also submit a complete list of medical devices manufactured for commercial distribution in the U.S. market.
All facilities that fall under any of the following functions:
- Contract Manufacturer
- Contract Sterilizer
- Foreign Exporter
- Manufacturer
- Relabeler / Repackager
- Remanufacturer
- Reprocessor of Single Use Device
- Specification Developer
- U.S. manufacturer of export only devices
What information is submitted for a medical device listing?
Medical device establishments must list any medical device made in the establishment and the activities the device is meant for.
- Company function (activity)
- Device product code
- Proprietary names
- Importer information
What is a master file?
A Master File is a secure, confidential submission of proprietary product data to a regulatory agency, such as the U.S. Food and Drug Administration (FDA), Health Canada, or the National Medical Products Association (NMPA) in China.