Safety announcements from medical device manufacturers From Danish Medicines Agency (DKMA) 🇩🇰 Number of entries: 5284 Metadata quality: Metadata quality: Data description empty Files documentation missing License filled Update frequency 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 today Other (Public Domain) 0 reuses 0 favorites
Safety information From National Agency for the Safety of Medicines and Health Products (ANSM) 🇫🇷 Safety information from the French Agency for the Safety of Medicines and Health Products Metadata quality: Metadata quality: Data description empty Files documentation missing License filled Update frequency 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 today Other (Non-Commercial) 0 reuses 0 favorites
Recalls and safety alerts From Health Canada 🇨🇦 Recall: 3798 results available. Alert: 17 results available Metadata quality: Metadata quality: Data description empty Files documentation missing License filled Update frequency 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 today Open Government License 2.0 (Canada) 0 reuses 0 favorites
List of recalls and other field safety corrective actions (FSCA) From Swiss Agency for Therapeutic Products (Swissmedic) 🇨🇭 Field safety information from Swissmedic: 10024 publications. Metadata quality: Metadata quality: Data description empty Files documentation missing License filled Update frequency 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 today Other (Non-Commercial) 0 reuses 0 favorites
Recalls of medical devices From National Organization for Medicines (EOF) 🇬🇷 Number of entries: 714 Metadata quality: Metadata quality: Data description empty Files documentation missing License filled Update frequency 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 1 day ago Other (Public Domain) 0 reuses 0 favorites
Alerts From Brazilian Health Regulatory Agency (Anvisa) 🇧🇷 Find the alerts published by Anvisa on products subject to health surveillance Metadata quality: Metadata quality: Data description empty Files documented License filled Update frequency followed File formats are open Temporal coverage not set Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 77.77777777777779/100 Updated 1 day ago Other (Public Domain) 0 reuses 0 favorites
Medical Device Recalls From Food and Drug Administration (FDA) 🇺🇸 Summaries of information about the most serious medical device recalls. These products are on the list because there is a reasonable chance that they could cause serious health problems or death. 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 14, 2024 Other (Public Domain) 0 reuses 0 favorites
Safety Alerts on Medical Devices From Ministry of Health (Italy) (MDS) 🇮🇹 Safety Alerts on Medical Devices Metadata quality: Metadata quality: Data description empty Files documentation missing License filled Update frequency 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 1 day ago Creative Commons Attribution 3.0 0 reuses 0 favorites
MHRA Strategy for Improving Safety Communications From Medicines and Healthcare products Regulatory Agency (MHRA) 🇬🇧 The MHRA’s strategy for Improving Safety Communications for 2024 to 2027. 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 2 days ago Open Government Licence 2.0 (United Kingdom) 0 reuses 0 favorites
Medical Devices; Immunology and Microbiology Devices; Classification of the Quantitative Viral Nucleic Acid Test for Transplant Patient Management From Food and Drug Administration (FDA) 🇺🇸 Document number 2024-21086. The Food and Drug Administration (FDA, Agency, or we) is classifying the quantitative viral nucleic acid test for transplant patient management into class II (special controls). The special controls that apply to the device type are identified in this order and will be… 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 days ago Other (Public Domain) 0 reuses 0 favorites
Medical Devices; Therapeutic Devices; Classification of the Pediatric Continuous Renal Replacement Therapy System From Food and Drug Administration (FDA) 🇺🇸 Document number 2024-20999. The Food and Drug Administration (FDA, Agency, or we) is classifying the pediatric continuous renal replacement therapy system into class II (special controls). The special controls that apply to the device type are identified in this order and will be part of the… 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 3 days ago Other (Public Domain) 0 reuses 0 favorites
Medical Devices; Immunology and Microbiology Devices; Classification of the Device To Detect or Measure Nucleic Acid From Viruses Associated With Head and Neck Cancers From Food and Drug Administration (FDA) 🇺🇸 Document number 2024-20896. The Food and Drug Administration (FDA, Agency, or we) is classifying the device to detect or measure nucleic acid from viruses associated with head and neck cancers into class II (special controls). The special controls that apply to the device type are identified in… 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 3 days ago Other (Public Domain) 0 reuses 0 favorites
Medical Devices; Clinical Chemistry and Clinical Toxicology Devices; Classification of the Clozapine Test System From Food and Drug Administration (FDA) 🇺🇸 Document number 2024-20895. The Food and Drug Administration (FDA, Agency, or we) is classifying the clozapine test system into class II (special controls). The special controls that apply to the device type are identified in this order and will be part of the codified language for the clozapine… 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 3 days ago Other (Public Domain) 0 reuses 0 favorites
Weekly reports of the National Center for Medical Devices and Products Reporting From Saudi Food and Drug Authority (SFDA) 🇸🇦 Weekly reports on safety alerts, recalls, and FSCAs from the National Center for Medical Devices and Products Reporting. 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 4 days ago Other (Public Domain) 0 reuses 0 favorites
Alerts and recalls of medical products - ANMAT From National Administration of Drugs, Food and Medical Devices (ANMAT) 🇦🇷 Stay informed about safety alerts and recalls of medical products with ANMAT's comprehensive database. 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 1 week ago Creative Commons Attribution 4.0 0 reuses 0 favorites
Medical Devices; Immunology and Microbiology Devices; Classification of the Whole Exome Sequencing Constituent Device From Food and Drug Administration (FDA) 🇺🇸 Document number 2024-20550. The Food and Drug Administration (FDA, Agency, or we) is classifying the whole exome sequencing constituent device into class II (special controls). The special controls that apply to the device type are identified in this order and will be part of the codified language… 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 1 week ago Other (Public Domain) 0 reuses 0 favorites
Medical Devices; Gastroenterology-Urology Devices; Classification of the Endoscopic Pancreatic Debridement Device From Food and Drug Administration (FDA) 🇺🇸 Document number 2024-20248. The Food and Drug Administration (FDA or we) is classifying the endoscopic pancreatic debridement device into class II (special controls). The special controls that apply to the device type are identified in this order and will be part of the codified language for the… 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 1 week ago Other (Public Domain) 0 reuses 0 favorites
Medical Devices; Clinical Chemistry and Clinical Toxicology Devices; Classification of the Blood Collection Device for Cell-Free Nucleic Acids From Food and Drug Administration (FDA) 🇺🇸 Document number 2024-20254. The Food and Drug Administration (FDA, Agency, or we) is classifying the blood collection device for cell-free nucleic acids into class II (special controls). The special controls that apply to the device type are identified in this order and will be part of the… 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 1 week ago Other (Public Domain) 0 reuses 0 favorites
Guidance for Industry: Preparing a Color Additive Petition for Submission to the Center for Food Safety and Applied Nutrition for Color Additives Used in or on Contact Lenses From Food and Drug Administration (FDA) 🇺🇸 A guidance document providing instructions for submitting a color additive petition for contact lenses to the Center for Food Safety and Applied Nutrition. Metadata quality: Metadata quality: Data description filled Files documentation missing License filled Update frequency not followed File formats are closed Temporal coverage filled Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 66.66666666666666/100 Updated 1 week ago Other (Public Domain) 0 reuses 0 favorites
Medical Devices; Gastroenterology-Urology Devices; Classification of the Hemodialyzer With Expanded Solute Removal Profile From Food and Drug Administration (FDA) 🇺🇸 Document number 2024-20081. The Food and Drug Administration (FDA or we) is classifying the hemodialyzer with expanded solute removal profile into class II (special controls). The special controls that apply to the device type are identified in this order and will be part of the codified language… 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 Other (Public Domain) 0 reuses 0 favorites