21 CFR Chapter I Subchapter H – Medical Devices – Part 864 Hematology and Pathology Devices From Food and Drug Administration (FDA) 🇺🇸 This document is a regulation titled "21 CFR Chapter I Subchapter H – Medical Devices – Part 864 Hematology and Pathology Devices". Metadata quality: Metadata quality: Data description filled Files documented 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: 77.77777777777779/100 Updated 2 weeks ago Other (Public Domain) 0 reuses 0 favorites
CPG Sec. 110.700 Seizures by the U.S. Customs Service of Prohibited Articles of Foreign Origin Not Intended for Entry into the United States From Food and Drug Administration (FDA) 🇺🇸 This document is a Compliance Policy Guide (CPG) titled "Seizures by the U.S. Customs Service of Prohibited Articles of Foreign Origin". 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 on September 29, 2023 Other (Public Domain) 0 reuses 0 favorites
CPG Sec. 110.600 FDA Authority Over Products of Foreign Origin Located in Foreign Trade Zones, Bonded Warehouses or on Bonded Carriers From Food and Drug Administration (FDA) 🇺🇸 This document discusses FDA's authority over foreign products in foreign trade zones, bonded warehouses, or on bonded carriers. 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 on September 29, 2023 Other (Public Domain) 0 reuses 0 favorites
Government response to report on Brexit and medicines, medical devices and substances of human origin From Medicines and Healthcare products Regulatory Agency (MHRA) 🇬🇧 Command paper responding to the Health and Social Care Committee's report 'Brexit: medicines, medical devices and substances of human origin'. 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 May 23, 2018 Open Government Licence 2.0 (United Kingdom) 0 reuses 0 favorites
The Medical Devices (Amendment) Regulations 2013 From Medicines and Healthcare products Regulatory Agency (MHRA) 🇬🇧 These Regulations amend the Medical Devices Regulation 2002 (the 2002 Regulations) in order to implement Commission Regulation (EU) No 207/2012 of 9 March 2012 on electronic instructions for use of medical devices and Commission Regulation (EU) No 722/2012 of 8 August 2012 concerning particular… 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 September 12, 2013 Open Government Licence 3.0 (United Kingdom) 0 reuses 0 favorites
Commission Regulation (EU) No 722/2012 of 8 August 2012 concerning particular requirements as regards the requirements laid down in Council Directives 90/385/EEC and 93/42/EEC with respect to active implantable medical devices and medical devices manufactured utilising tissues of animal origin Text with EEA relevance From European Parliament 🇪🇺 Commission Regulation (EU) No. 722/2012 sets specific requirements for active implantable medical devices and medical devices made from animal tissues. 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 August 8, 2012 Creative Commons Attribution 4.0 0 reuses 0 favorites
On the issuance of passive implantable and animal origin medical device registration declaration information guidelines notice From National Medical Products Administration (NMPA) 🇨🇳 FGWJ-2010-10011 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 December 30, 2009 Other (Public Domain) 0 reuses 0 favorites
Order of December 4, 2006 amending the decree of September 13, 2005 concerning the detailed specifications specifying the essential requirements with which medical devices manufactured from tissues of animal origin must comply From Ministry of Labor, Health and Solidarity (MTSS) 🇫🇷 Document NOR : SANP0624888A – Arrêté du 4 décembre 2006 modifiant l'arrêté du 13 septembre 2005 relatif aux spécifications détaillées précisant les exigences essentielles auxquelles doivent se conformer les dispositifs médicaux fabriqués à partir de tissus d'origine animale 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 December 4, 2006 Other (Public Domain) 0 reuses 0 favorites
Announcement on the Registration of Medical Devices Containing Materials of Bovine and Sheep Origin From National Medical Products Administration (NMPA) 🇨🇳 FGWJ-2006-10041 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 2, 2006 Other (Public Domain) 0 reuses 0 favorites
Order of September 13, 2005 concerning the detailed specifications specifying the essential requirements with which medical devices manufactured from tissues of animal origin must comply (correction) From Ministry of Labor, Health and Solidarity (MTSS) 🇫🇷 Document NOR : SANP0522988Z – Arrêté du 13 septembre 2005 relatif aux spécifications détaillées précisant les exigences essentielles auxquelles doivent se conformer les dispositifs médicaux fabriqués à partir de tissus d'origine animale (rectificatif) 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 September 13, 2005 Other (Public Domain) 0 reuses 0 favorites
Order of September 13, 2005 concerning the detailed specifications specifying the essential requirements with which medical devices manufactured from tissues of animal origin must comply From Ministry of Labor, Health and Solidarity (MTSS) 🇫🇷 Document NOR : SANP0522988A – Arrêté du 13 septembre 2005 relatif aux spécifications détaillées précisant les exigences essentielles auxquelles doivent se conformer les dispositifs médicaux fabriqués à partir de tissus d'origine animale 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 September 13, 2005 Other (Public Domain) 0 reuses 0 favorites
Corrigendum to Commission Directive 2003/32/EC of 23 April 2003 introducing detailed specifications as regards the requirements laid down in Council Directive 93/42/EEC with respect to medical devices utilising tissues of animal origin (OJ L 105, 26.4.2003) From European Parliament 🇪🇺 Corrigendum to Commission Directive 2003/32/EC amends requirements for medical devices using animal tissues, as per Council Directive 93/42/EEC. 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 8, 2005 Creative Commons Attribution 4.0 0 reuses 0 favorites
The Medical Devices (Amendment) Regulations 2003 From Medicines and Healthcare products Regulatory Agency (MHRA) 🇬🇧 These Regulations amend the Medical Devices Regulations 2002 (“the principal Regulations”), which contain the legislative measures necessary for the implementation of the European Community scheme for regulating the placing on the market and putting into service of medical devices. The amendments… 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 September 1, 2003 Open Government Licence 3.0 (United Kingdom) 0 reuses 0 favorites
Commission Directive 2003/32/EC of 23 April 2003 introducing detailed specifications as regards the requirements laid down in Council Directive 93/42/EEC with respect to medical devices manufactured utilising tissues of animal origin (Text with EEA relevance) From European Parliament 🇪🇺 Commission Directive 2003/32/EC introduces specifications for medical devices made from animal tissues, in accordance with Council Directive 93/42/EEC. 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 23, 2003 Creative Commons Attribution 4.0 0 reuses 0 favorites
S.I. No. 554/2003 - European Communities (Medical Devices) (Tissues of Animal Origin) Regulations, 2003 From Health Products Regulatory Authority (HPRA) 🇮🇪 A statutory instrument from 2003, focusing on regulations for medical devices made from tissues of animal origin within the European Communities. 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 8, 2024 Other (Public Domain) 0 reuses 0 favorites