21 CFR Chapter I Subchapter H โ Medical Devices โ Part 884 Obstetrical and Gynecological 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 884 Obstetrical and Gynecological 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 on March 31, 2023 Other (Public Domain) 0 reuses 0 favorites
Notification on the Supervision and Inspection of the Product Quality of Disposable Sterile Vaginal Dilators From National Medical Products Administration (NMPA) ๐จ๐ณ FGWJ-2005-10191 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
Letter on the Release of YY 0336-2002 "Single-use Sterile Vaginal Dilator" Medical Device Industry Standard No. 1 Revision Sheet From National Medical Products Administration (NMPA) ๐จ๐ณ FGWJ-2004-10163 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 October 11, 2004 Other (Public Domain) 0 reuses 0 favorites
Notice on the release of the industry standard of "Single-use sterile vaginal dilator". From National Medical Products Administration (NMPA) ๐จ๐ณ FGWJ-2002-10162 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 24, 2002 Other (Public Domain) 0 reuses 0 favorites
Medical Devices; Effective Date of Requirement for Premarket Approval for Three Preamendment Class III Devices From Food and Drug Administration (FDA) ๐บ๐ธ Document number 00-9135. The Food and Drug Administration (FDA) is issuing a final rule to retain three class III preamendment devices in class III and to require the filing of a premarket approval application (PMA) or a notice of completion of a product development protocol (PDP) for 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 April 13, 2000 Other (Public Domain) 0 reuses 0 favorites
Vaginal Mesh Implants From Health Products Regulatory Authority (HPRA) ๐ฎ๐ช A document discussing concerns related to vaginal mesh implants. 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 8, 2024 Other (Public Domain) 0 reuses 0 favorites