21 CFR Chapter I Subchapter H – Medical Devices – Part 876 Gastroenterology-Urology Devices From Food and Drug Administration (FDA) 🇺🇸 Regulation on Gastroenterology-Urology Devices under 21 CFR Chapter I Subchapter H - Medical Devices, Part 876. 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 days ago Other (Public Domain) 0 reuses 0 favorites
21 CFR Chapter I Subchapter H – Medical Devices – Part 886 Ophthalmic Devices From Food and Drug Administration (FDA) 🇺🇸 This document is a regulation titled "21 CFR Chapter I Subchapter H – Medical Devices – Part 886 Ophthalmic 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
21 CFR Chapter I Subchapter H – Medical Devices – Part 872 Dental Devices From Food and Drug Administration (FDA) 🇺🇸 This document is a regulation titled "21 CFR Chapter I Subchapter H – Medical Devices – Part 872 Dental 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
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
Medical Devices; Hematology and Pathology Devices; Classification of the Heparin and Direct Oral Factor Xa Inhibitor Drug Test System From Food and Drug Administration (FDA) 🇺🇸 Document number 2024-19824. The Food and Drug Administration (FDA or we) is classifying the heparin and direct oral factor Xa inhibitor drug 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… 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
About the shortage of oral cefalexin From Therapeutic Goods Administration (TGA) 🇦🇺 Read about how the shortage of oral cefalexin products, that started in December 2022, now only applies to syrups and suspensions. 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 31, 2023 Other (Non-Commercial) 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
State Drug Administration Comprehensive Department on the consent to prepare for the establishment of oral digital medical device standardization technology focal point unit of the reply letter From National Medical Products Administration (NMPA) 🇨🇳 FGWJ-2022-164 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 March 10, 2024 Other (Public Domain) 0 reuses 0 favorites
Oral Drug Products Administered Via Enteral Feeding Tube: In Vitro Testing and Labeling Recommendations: Draft Guidance for Industry From Food and Drug Administration (FDA) 🇺🇸 Draft guidance document providing recommendations for in vitro testing and labeling of oral drug products administered via enteral feeding tube. 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 February 1, 2022 Other (Public Domain) 0 reuses 0 favorites
Prospective Manufacturers of Barrier Devices Used During Oral Sex for STD Protection From Food and Drug Administration (FDA) 🇺🇸 A guidance document for manufacturers of barrier devices used during oral sex to protect against STDs. 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 March 24, 2020 Other (Public Domain) 0 reuses 0 favorites
Restricted Delivery Systems: Flow Restrictors for Oral Liquid Drug Products Guidance for Industry From Food and Drug Administration (FDA) 🇺🇸 Guidance document on flow restrictors for oral liquid drug products, focusing on restricted delivery systems. Title: Restricted Delivery Systems: Flow Restrictors for Oral Liquid Drug Products Guidance for Industry. 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 March 17, 2020 Other (Public Domain) 0 reuses 0 favorites
Medical Devices; Dental Devices; Classification of the Auto Titration Device for Oral Appliances From Food and Drug Administration (FDA) 🇺🇸 Document number 2019-02824. The Food and Drug Administration (FDA or we) is classifying the auto titration device for oral appliances 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 on February 20, 2019 Other (Public Domain) 0 reuses 0 favorites
Medical Devices; Gastroenterology-Urology Devices; Classification of the Oral Removable Palatal Space Occupying Device for Weight Management and/or Weight Loss From Food and Drug Administration (FDA) 🇺🇸 Document number 2017-15894. The Food and Drug Administration (FDA or Agency) is classifying the oral removable palatal space occupying device for weight management and/or weight loss into class II (special controls). The special controls that will apply to the device are identified in this order… 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 28, 2017 Other (Public Domain) 0 reuses 0 favorites
Medical Devices; Ophthalmic Devices; Classification of the Oral Electronic Vision Aid From Food and Drug Administration (FDA) 🇺🇸 Document number 2015-24026. The Food and Drug Administration (FDA) is classifying the oral electronic vision aid into class II (special controls). The special controls that will apply to the device are identified in this order and will be part of the codified language for the oral electronic… 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 22, 2015 Other (Public Domain) 0 reuses 0 favorites
Notice on the Accreditation of Shanghai Biomaterials Research and Testing Center for Testing of Medical Devices, Oral Materials and Biomaterials Evaluation and Testing Projects From National Medical Products Administration (NMPA) 🇨🇳 FGWJ-2012-10185 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 June 6, 2012 Other (Public Domain) 0 reuses 0 favorites
Notice on the Accreditation of Shanghai Biomaterials Research and Testing Center for Biological Evaluation and Testing of Medical Devices and Oral Appliances and other 2 items of testing qualifications From National Medical Products Administration (NMPA) 🇨🇳 FGWJ-2008-10050 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 April 16, 2008 Other (Public Domain) 0 reuses 0 favorites
Notification of the definition of the classification of products such as oral digital viewers, etc. From National Medical Products Administration (NMPA) 🇨🇳 FGWJ-2005-10178 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 April 15, 2005 Other (Public Domain) 0 reuses 0 favorites
Notice on the release of 19 industry standards, including Oral X-ray Machine From National Medical Products Administration (NMPA) 🇨🇳 FGWJ-2002-10184 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 September 24, 2002 Other (Public Domain) 0 reuses 0 favorites
Notice on regulating the supervision and management of the production of oral prostheses From National Medical Products Administration (NMPA) 🇨🇳 FGWJ-2002-10123 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 September 17, 2002 Other (Public Domain) 0 reuses 0 favorites
Notice on the Publication of Four Industry Standards, including "Preclinical Evaluation of Biocompatibility of Medical Devices for Oral Use Unit 1: Evaluation and Test Item Selection From National Medical Products Administration (NMPA) 🇨🇳 FGWJ-2001-10192 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 November 9, 2001 Other (Public Domain) 0 reuses 0 favorites