21 CFR Chapter I Subchapter H โ Medical Devices โ Part 888 Orthopedic Devices From Food and Drug Administration (FDA) ๐บ๐ธ This document is a regulation titled "21 CFR Chapter I Subchapter H โ Medical Devices โ Part 888 Orthopedic 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
Defining joint replacement medical devices and ancillary medical devices From Therapeutic Goods Administration (TGA) ๐ฆ๐บ Guidance for manufacturers and sponsors on shoulder, hip and knee joint replacement medical devices and ancillary medical devices. 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 27, 2024 Other (Non-Commercial) 0 reuses 0 favorites
Medical Devices; Orthopedic Devices; Classification of the Implantable Post-Surgical Kinematic Measurement Knee Device From Food and Drug Administration (FDA) ๐บ๐ธ Document number 2022-28604. The Food and Drug Administration (FDA, Agency or we) is classifying the implantable post-surgical kinematic measurement knee 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 theโฆ 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 5, 2023 Other (Public Domain) 0 reuses 0 favorites
KNEE ACTIVE PLUS From National Organization for Medicines (EOF) ๐ฌ๐ท The EOF draws the attention of consumers, because the product ฮฮKNEE ACTIVE PLUSฮฮ is advertised and distributed online for a variety of therapeutic uses, ... 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 29, 2021 Other (Public Domain) 0 reuses 0 favorites
Provision No. 539/12 From National Administration of Drugs, Food and Medical Devices (ANMAT) ๐ฆ๐ท The "Official List of Implants Released for Commercialization and Use" (LOI) is created. The list shall cover the following products: breast implants, hip prostheses, knee prostheses and spine implants. B.O. January 31, 2012. 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 January 1, 2012 Creative Commons Attribution 4.0 0 reuses 0 favorites
Commission Directive 2005/50/EC of 11 August 2005 on the reclassification of hip, knee and shoulder joint replacements in the framework of Council Directive 93/42/EEC concerning medical devices (Text with EEA relevance) From European Parliament ๐ช๐บ Commission Directive 2005/50/EC reclassifies hip, knee, and shoulder joint replacements under Council Directive 93/42/EEC on medical devices. 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 11, 2005 Creative Commons Attribution 4.0 0 reuses 0 favorites
Notice on the Investigation and Handling of Unqualified and Unlicensed Artificial Hip (Knee) Joint Products From National Medical Products Administration (NMPA) ๐จ๐ณ FGWJ-2002-10334 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
S.I. No. 92/2007 - European Communities (Medical Devices) (Reclassification of Hip, Knee and Shoulder Joint Replacements) (Amendment) Regulations 2007 From Health Products Regulatory Authority (HPRA) ๐ฎ๐ช A statutory instrument from 2007 amending regulations related to the reclassification of hip, knee, and shoulder joint replacements in 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