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
21 CFR Chapter I Subchapter H – Medical Devices – Part 880 General Hospital and Personal Use Devices From Food and Drug Administration (FDA) 🇺🇸 21 CFR Chapter I Subchapter H - Medical Devices - Part 880 General Hospital and Personal Use Devices. Regulation. 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 on August 19, 2024 Other (Public Domain) 0 reuses 0 favorites
Chapter 10 - general advice on vigilance - Great Britain From Medicines and Healthcare products Regulatory Agency (MHRA) 🇬🇧 Collecting and acting on information on any adverse effects of electronic cigarette devices and refill containers on human health. 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 16, 2024 Open Government Licence 2.0 (United Kingdom) 0 reuses 0 favorites
Medical Devices; Hematology and Pathology Devices; Classification of the Container System for the Processing and Storage of Red Blood Cell Components Under Reduced Oxygen Conditions From Food and Drug Administration (FDA) 🇺🇸 Document number 2023-24717. The Food and Drug Administration (FDA, Agency, or we) is classifying the container system for the processing and storage of Red Blood Cell components under reduced oxygen conditions into class II (special controls). The special controls that apply to the device type are… 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 9, 2023 Other (Public Domain) 0 reuses 0 favorites
Chapter 9 - General advice on due diligence Northern Ireland From Medicines and Healthcare products Regulatory Agency (MHRA) 🇬🇧 General advice on due diligence - electronic cigarettes devices and refill containers. 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 March 23, 2022 Open Government Licence 2.0 (United Kingdom) 0 reuses 0 favorites
Chapter 10 - General Advice on Vigilance - Northern Ireland From Medicines and Healthcare products Regulatory Agency (MHRA) 🇬🇧 General advice on vigilance - electronic cigarettes devices and refill containers. 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 March 23, 2022 Open Government Licence 2.0 (United Kingdom) 0 reuses 0 favorites
Container and Closure System Integrity Testing in Lieu of Sterility Testing as a Component of the Stability Protocol for Sterile Products: Guidance for Industry From Food and Drug Administration (FDA) 🇺🇸 This document provides guidance on using container and closure system integrity testing instead of sterility testing for stability protocols of sterile products. 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 May 6, 2020 Other (Public Domain) 0 reuses 0 favorites
Guidance on the Content and Format of Premarket Notification [510(k)] Submissions for Sharps Containers From Food and Drug Administration (FDA) 🇺🇸 A guidance document providing instructions for the content and format of premarket notification submissions for sharps containers. 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
Selection of the Appropriate Package Type Terms and Recommendations for Labeling Injectable Medical Products Packaged in Multiple-Dose, Single-Dose, and Single-Patient-Use Containers for Human Use: Guidance for Industry From Food and Drug Administration (FDA) 🇺🇸 This is a guidance document titled "Selection of the Appropriate Package Type Terms and Recommendations for Labeling Injectable Medical Products Packaged in Multiple-Dose, Single-Dose, and Single-Patient-Use Containers for Human Use: Guidance for Industry". It covers topics like CMC, combination… 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 May 31, 2019 Other (Public Domain) 0 reuses 0 favorites
Recommendations for Labeling Medical Products to Inform Users that the Product or Product Container is not Made with Natural Rubber Latex: Guidance for Industry and Food and Drug Administration Staff From Food and Drug Administration (FDA) 🇺🇸 This document provides guidance for labeling medical products to inform users that they are not made with natural rubber latex. 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 14, 2019 Other (Public Domain) 0 reuses 0 favorites
Food and Drug Administration on the recognition of medical devices and pharmaceutical packaging materials (containers) testing laboratory in Hunan Province, medical device testing object testing qualification notice From National Medical Products Administration (NMPA) 🇨🇳 FGWJ-2014-10122 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
On the accreditation of Hunan Medical Devices and Pharmaceutical Packaging Materials (Containers) Testing Institute for single-use sterile syringes and other medical devices and project testing qualifications notice From National Medical Products Administration (NMPA) 🇨🇳 FGWJ-2010-10294 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 23, 2010 Other (Public Domain) 0 reuses 0 favorites
Notice of Transmittal of Revision Sheet No. 1 to the National Standard for Bagged Plastic Containers for Human Blood and Blood Components, Part 1: Traditional Blood Bags From National Medical Products Administration (NMPA) 🇨🇳 FGWJ-2007-10068 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 3, 2007 Other (Public Domain) 0 reuses 0 favorites
On the implementation of YY0314-2007 "disposable use of human venous blood sample collection container" and other 18 medical device industry standards notice From National Medical Products Administration (NMPA) 🇨🇳 FGWJ-2007-10101 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 July 2, 2007 Other (Public Domain) 0 reuses 0 favorites
On the accreditation of Hunan Medical Devices and Pharmaceutical Packaging Materials (Containers) Testing Institute of guitars and other products and projects testing qualification notice From National Medical Products Administration (NMPA) 🇨🇳 FGWJ-2007-10533 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 May 18, 2007 Other (Public Domain) 0 reuses 0 favorites
Hematology and Pathology Devices; Reclassification; Restricted Devices; OTC Test Sample Collection Systems for Drugs of Abuse Testing From Food and Drug Administration (FDA) 🇺🇸 Document number 00-8598. The Food and Drug Administration (FDA) is reclassifying over- the-counter (OTC) test sample collection systems for drugs of abuse testing from class III (premarket approval) into class I (general controls) and exempting them from premarket notification (510(k)) and current… 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 7, 2000 Other (Public Domain) 0 reuses 0 favorites