Commission Implementing Decision (EU) 2024/815 of 6 March 2024 amending Implementing Decision (EU) 2021/1182 as regards harmonised standards for medical gloves for single use, biological evaluation of medical devices, sterilization of health care products, packaging for terminally sterilized medical devices and processing of health care products From European Parliament 🇪🇺 The document is a Commission Implementing Decision amending standards for medical gloves, biological evaluation of devices, sterilization, packaging, and processing of healthcare products. 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 6, 2024 Creative Commons Attribution 4.0 0 reuses 0 favorites
Medical Devices; General and Plastic Surgery Devices; Reclassification of Blood Lancets From Food and Drug Administration (FDA) 🇺🇸 Document number 2021-25376. The Food and Drug Administration (FDA or the Agency) is issuing a final order to reclassify three types of blood lancets used to puncture skin to obtain a drop of blood for diagnostic purposes from class I (general controls) exempt from premarket notification into class… 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 November 22, 2021 Other (Public Domain) 0 reuses 0 favorites
Reprocessing of Single Use Medical Devices Communication to Stakeholders From South African Health Products Regulatory Authority (SAHPRA) 🇿🇦 Version 1 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 November 20, 2019 Other (Public Domain) 0 reuses 0 favorites
General and Plastic Surgery Devices; Reclassification of Blood Lancets From Food and Drug Administration (FDA) 🇺🇸 Document number 2016-04578. The Food and Drug Administration (FDA or the Agency) is proposing to reclassify the following three types of blood lancets used to puncture skin to obtain a drop of blood for diagnostic purposes from class I (general controls) exempt from premarket notification into… 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 3, 2016 Other (Public Domain) 0 reuses 0 favorites
Provision No. 2323/02 From National Administration of Drugs, Food and Medical Devices (ANMAT) 🇦🇷 MERCOSUR Technical Regulations on Sterile Hypodermic Syringes for Single Use - BO 21/06/02 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 1, 2002 Creative Commons Attribution 4.0 0 reuses 0 favorites