ESSURE® device information From Spanish Agency for Medicines and Medical Devices (AEMPS) 🇪🇸 Last update: July 11, 2019 Informative Notes Web Publication Document Title 10/16/18 María Luisa Carcedo presents the Action Guide for patients carrying the Essure® contraceptive Press Release 10/16/18 Publication of the action guide for a patient carrying the Essure® device PS Informative Note,... 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 June 10, 2024 Other (Public Domain) 0 reuses 0 favorites
21 CFR Chapter I Subchapter H – Medical Devices – Part 884 Obstetrical and Gynecological Devices From Food and Drug Administration (FDA) 🇺🇸 This document is a regulation titled "21 CFR Chapter I Subchapter H – Medical Devices – 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
Uniform Contraceptive Labeling - Guidance for Industry From Food and Drug Administration (FDA) 🇺🇸 This document is a guidance for the industry on premarket requirements for uniform contraceptive labeling. 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 18, 2020 Other (Public Domain) 0 reuses 0 favorites
Obstetrical and Gynecological Devices; Classification of Female Condoms From Food and Drug Administration (FDA) 🇺🇸 Document number 00-12526. The Food and Drug Administration (FDA) is classifying the preamendments female condom intended for contraceptive and prophylactic purposes. Under this rule, the preamendments female condom is being classified into class III (premarket approval). This action is being taken… 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 18, 2000 Other (Public Domain) 0 reuses 0 favorites