Assistive technology: definitions, examples and safe use From Medicines and Healthcare products Regulatory Agency (MHRA) 🇬🇧 Helps manufacturers and healthcare professionals understand the definition of assistive technology and the difference between medical devices and aids to daily living. Metadata quality: Metadata quality: Data description filled Files documentation missing License filled Update frequency not followed File formats are open Temporal coverage not set Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 66.66666666666666/100 Updated 2 weeks ago Open Government Licence 2.0 (United Kingdom) 0 reuses 0 favorites
Software and artificial intelligence (AI) as a medical device From Medicines and Healthcare products Regulatory Agency (MHRA) 🇬🇧 Information for manufacturers, healthcare professionals, researchers and patients on software as a medical device (SaMD) and AI as a medical device (AIaMD). Metadata quality: Metadata quality: Data description filled Files documentation missing License filled Update frequency not followed File formats are open Temporal coverage not set Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 66.66666666666666/100 Updated on June 13, 2024 Open Government Licence 2.0 (United Kingdom) 0 reuses 0 favorites
Alerts - Medical Devices From Spanish Agency for Medicines and Medical Devices (AEMPS) 🇪🇸 Last updated: December 20, 2018 The purpose of medical device alerts is to bring to the attention of healthcare professionals and/or users of such devices, the potential risks that may arise from their use and the measures to be taken to minimize or eliminate them.... Metadata quality: Metadata quality: Data description filled Files documentation missing License filled Update frequency not followed File formats are open Temporal coverage not set Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 66.66666666666666/100 Updated on June 10, 2024 Other (Public Domain) 0 reuses 0 favorites
UDI: resources and technical documents From Therapeutic Goods Administration (TGA) 🇦🇺 Resources and technical documents for sponsors, manufacturers, consumers, and healthcare professionals. Metadata quality: Metadata quality: Data description filled Files documentation missing License filled Update frequency not followed File formats are open Temporal coverage not set Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 66.66666666666666/100 Updated on May 29, 2024 Other (Non-Commercial) 0 reuses 0 favorites
Squamous cell carcinoma (SCC) and different types of lymphomas occurring in the capsule around breast implants From Medicines and Healthcare products Regulatory Agency (MHRA) 🇬🇧 Information for healthcare professionals, patients, and the public. Metadata quality: Metadata quality: Data description empty Files documentation missing License filled Update frequency not followed File formats are open Temporal coverage not set Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 55.55555555555556/100 Updated on August 7, 2023 Open Government Licence 2.0 (United Kingdom) 0 reuses 0 favorites
Reporting system for in vitro diagnostic medical devices From Ministry of Health (Italy) (MDS) 🇮🇹 The Ministry of Health carries out the activities of monitoring and investigating reports from healthcare professionals and manufacturers. On Sept. 28, 2022, Legislative Decree No. 138 of Aug. 5, 2022 , came into force, which in Article 13 provides fulfillments for manufacturers of in vitro… Metadata quality: Metadata quality: Data description filled Files documentation missing License filled Update frequency not followed File formats are open Temporal coverage not set Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 66.66666666666666/100 Updated on July 3, 2023 Creative Commons Attribution 3.0 0 reuses 0 favorites
Adrenaline Auto-Injectors (AAIs) safety campaign From Medicines and Healthcare products Regulatory Agency (MHRA) 🇬🇧 Information for patients, healthcare professionals and the wider public to help better understand the importance of AAIs as a potential life-saving medicine. Metadata quality: Metadata quality: Data description filled Files documentation missing License filled Update frequency not followed File formats are open Temporal coverage not set Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 66.66666666666666/100 Updated on June 19, 2023 Open Government Licence 2.0 (United Kingdom) 0 reuses 0 favorites
How to draft a direct healthcare professional communication From Medicines and Healthcare products Regulatory Agency (MHRA) 🇬🇧 Guidance for marketing authorisation holders on drafting direct healthcare professional communications (DHPCs) Metadata quality: Metadata quality: Data description filled Files documentation missing License filled Update frequency not followed File formats are open Temporal coverage not set Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 66.66666666666666/100 Updated on April 4, 2023 Open Government Licence 2.0 (United Kingdom) 0 reuses 0 favorites
GN-09-R3.6 Guidance on the Component Elements of a DHCPL (2022 May) PUB From Health Sciences Authority (HSA) 🇸🇬 Provides guidance on creating Dear Healthcare Professional Letters (DHCPL). Metadata quality: Metadata quality: Data description empty Files documentation missing License filled Update frequency not followed File formats are closed Temporal coverage not set Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 44.44444444444444/100 Updated on May 1, 2022 Other (Public Domain) 0 reuses 0 favorites
Guidance for healthcare professionals and assistive device depots on medical device customization and custom device manufacturing From Danish Medicines Agency (DKMA) 🇩🇰 A document providing guidance for healthcare professionals and assistive device depots on customizing and manufacturing medical devices. Metadata quality: Metadata quality: Data description filled Files documentation missing License filled Update frequency not followed File formats are open Temporal coverage not set Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 66.66666666666666/100 Updated on October 28, 2021 Other (Public Domain) 0 reuses 0 favorites
Guidance for hospital operators, healthcare professionals and other medical device users on reporting medical device incidents From Danish Medicines Agency (DKMA) 🇩🇰 A document providing guidance for hospital operators, healthcare professionals, and medical device users on reporting medical device incidents. Metadata quality: Metadata quality: Data description filled Files documentation missing License filled Update frequency not followed File formats are open Temporal coverage not set Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 66.66666666666666/100 Updated on May 21, 2021 Other (Public Domain) 0 reuses 0 favorites
The use and regulation of pulse oximeters (information for healthcare professionals) From Medicines and Healthcare products Regulatory Agency (MHRA) 🇬🇧 Information for healthcare professionals on how pulse oximeters are regulated, home use and issues to look out for when using the devices Metadata quality: Metadata quality: Data description filled Files documentation missing License filled Update frequency not followed File formats are open Temporal coverage not set Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 66.66666666666666/100 Updated on March 26, 2021 Open Government Licence 2.0 (United Kingdom) 0 reuses 0 favorites
Single-use medical devices: implications and consequences of re-use From Medicines and Healthcare products Regulatory Agency (MHRA) 🇬🇧 Guidance for healthcare professionals on using single-use medical devices. Metadata quality: Metadata quality: Data description empty Files documentation missing License filled Update frequency not followed File formats are closed Temporal coverage not set Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 44.44444444444444/100 Updated on January 28, 2021 Open Government Licence 2.0 (United Kingdom) 0 reuses 0 favorites
The Yellow Card scheme: guidance for healthcare professionals, patients and the public From Medicines and Healthcare products Regulatory Agency (MHRA) 🇬🇧 Details of the Yellow Card scheme, which is the system for recording adverse incidents with medicines and medical devices in the UK. Metadata quality: Metadata quality: Data description filled Files documentation missing License filled Update frequency not followed File formats are open Temporal coverage not set Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 66.66666666666666/100 Updated on January 1, 2021 Open Government Licence 2.0 (United Kingdom) 0 reuses 0 favorites
Electrosurgery: top tips From Medicines and Healthcare products Regulatory Agency (MHRA) 🇬🇧 Top tips for healthcare professionals on safely managing electrosurgery from the Medicines and Healthcare products Regulatory Agency (MHRA). Metadata quality: Metadata quality: Data description filled Files documentation missing License filled Update frequency not followed File formats are closed Temporal coverage not set Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 55.55555555555556/100 Updated on November 17, 2015 Open Government Licence 2.0 (United Kingdom) 0 reuses 0 favorites
Blood pressure measurement devices From Medicines and Healthcare products Regulatory Agency (MHRA) 🇬🇧 Guidance for healthcare professionals on the use and management of blood pressure management devices. Metadata quality: Metadata quality: Data description filled Files documentation missing License filled Update frequency not followed File formats are closed Temporal coverage not set Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 55.55555555555556/100 Updated on December 1, 2013 Open Government Licence 2.0 (United Kingdom) 0 reuses 0 favorites
Devices: General Hospital and Personal Use Devices; Reclassification of Medical Device Data System From Food and Drug Administration (FDA) 🇺🇸 Document number E8-2325. The Food and Drug Administration (FDA) is proposing to reclassify, on its own initiative, the Medical Device Data System (MDDS) from class III (premarket approval) to class I (general controls). This action does not include medical device data systems with new diagnostic… Metadata quality: Metadata quality: Data description filled Files documentation missing License filled Update frequency not followed File formats are open Temporal coverage not set Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 66.66666666666666/100 Updated on February 8, 2008 Other (Public Domain) 0 reuses 0 favorites