Gefragt von: Ying Xiaming
Fragesteller Allgemeines

Fda Login Medical Device

Der Link der Fda Login Medical Device-Seite ist unten angegeben. Seiten, die sich auf Fda Login Medical Device beziehen, werden ebenfalls aufgelistet.

Zuletzt aktualisiert: 2022-02-02

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Added by: Penny Van Blommestein

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Investigational Device Exemption (IDE) | FDA

An investigational device exemption (IDE) allows the investigational device to be used in a clinical study in order to collect safety and effectiveness data required to support a Premarket ...
Url: https://www.fda.gov/medical-devices/premarket-submissions-selecting-and-preparing-correct-submission/investigational-device-exemption-ide
Investigational Device Exemption (IDE) | FDA

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Added by: Seepahn Ingilizian

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2022 Medical Device Recalls | FDA

28.01.2022 · 2022 Medical Device Recalls. Device Name. Date. Medtronic Inc. Recalls HawkOne Directional Atherectomy System Due to Risk of Tip Damage During Use. 01/21/22. Getinge USA Sales, LLC Recalls the ...
Url: https://www.fda.gov/medical-devices/medical-device-recalls/2022-medical-device-recalls
2022 Medical Device Recalls | FDA

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Added by: Alison Campagnolo

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FDA warns about Log4j cybersecurity vulnerabilities in ...

20.12.2021 · Log4j, which is used to log security and performance information, impacts upwards of 3 billion devices that use Java across a variety of consumer and enterprise services, websites and applications, as well as medical devices and supporting systems. FDA said manufacturers who may be affected by the vulnerabilities should communicate with their customers and …
Url: https://www.medtechdive.com/news/fda-warns-log4j-cybersecurity-risks-medical-devices/611773/
FDA warns about Log4j cybersecurity vulnerabilities in ...

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Added by: Krishan Kumar

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Transition Plan for Medical Devices Issued ... - fda.gov

23.12.2021 · FDA is issuing this guidance to describe FDA’s general recommendations for the transition process with respect to devices issued EUAs during the COVID-19 PHE.
Url: https://www.fda.gov/regulatory-information/search-fda-guidance-documents/transition-plan-medical-devices-issued-emergency-use-authorizations-euas-during-coronavirus-disease
Transition Plan for Medical Devices Issued ... - fda.gov

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Added by: Maria Sleight

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Dental Implants: What You Should Know | FDA

29.10.2021 · Dental implants are medical devices surgically implanted into the jaw to restore a person's ability to chew or their appearance. They provide …
Url: https://www.fda.gov/medical-devices/dental-devices/dental-implants-what-you-should-know
Dental Implants: What You Should Know | FDA

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Transition Plan for Medical Devices That Fall ... - fda.gov

The FDA draft guidance document “Transition Plan for Medical Devices Issued Emergency Use Authorizations (EUAs) During the Coronavirus Disease 2019 (COVID-19) …
Url: https://www.fda.gov/media/155038/download
Transition Plan for Medical Devices That Fall ... - fda.gov

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Added by: Emergo by UL Solutions

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United States Medical Device Registration Chapter 6 - Representation

Added by: Medical Device Academy

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FDA Establishment Registration and Listing for Medical Devices

Added by: Easy Medical Device

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How to register a Medical Device with FDA? (510k, PMA, de Novo...)

Added by: The BME Life

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Medical Device Regulations / FDA Approval

Added by: U.S. Food and Drug Administration

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An Introduction to FDA's Regulation of Medical Devices

Added by: Easy Medical Device

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How to register a Medical Device through FDA 510k with Michelle Lott

Added by: Exponential Medicine

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The FDA's Bakul Patel - Software as a Medical Device | Exponential Medicine

Added by: Registrar Corp

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FDA 101 for Medical Devices

Added by: MassMEDIC

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FDA Cybersecurity in Medical Devices

Added by: SpecialtyCare

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FDA Regulation of Medical Devices - Abridged and Simplified