21 CFR Chapter I Subchapter H β Medical Devices β Part 886 Ophthalmic Devices From Food and Drug Administration (FDA) πΊπΈ This document is a regulation titled "21 CFR Chapter I Subchapter H β Medical Devices β 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 β Medical Devices β Part 880 General Hospital and Personal Use Devices From Food and Drug Administration (FDA) πΊπΈ 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 1 month ago Other (Public Domain) 0 reuses 0 favorites
Principle 11: Protection against radiation From Therapeutic Goods Administration (TGA) π¦πΊ A medical device must be designed and produced in a way that ensures that the exposure of a patient, the user, or any other person, to radiation is minimised. 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 11, 2024 Other (Non-Commercial) 0 reuses 0 favorites
Guidance on SFDA Requirements for Quality Assurance Programs for Radiation Emitting and Imaging Devices (MDS-G15) From Saudi Food and Drug Authority (SFDA) πΈπ¦ Guidance on quality assurance programs for radiation emitting and imaging devices as per SFDA requirements. 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 September 28, 2023 Other (Public Domain) 0 reuses 0 favorites
21 CFR Chapter I Subchapter H β Medical Devices β Part 892 Radiology Devices From Food and Drug Administration (FDA) πΊπΈ This document is a regulation titled "21 CFR Chapter I Subchapter H β Medical Devices β Part 892 Radiology 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 June 7, 2023 Other (Public Domain) 0 reuses 0 favorites
National Diagnostic Reference Levels From Saudi Food and Drug Authority (SFDA) πΈπ¦ Reulgation setting standards for medical radiation exposure levels. 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 February 7, 2023 Other (Public Domain) 0 reuses 0 favorites
Guidance for the operation and use of radiation emitting medical devices (MDS β G007) From Saudi Food and Drug Authority (SFDA) πΈπ¦ Guidance for operating and using radiation emitting medical devices. 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 December 22, 2022 Other (Public Domain) 0 reuses 0 favorites
Response letter from the Comprehensive Department of the State Drug Administration on the management attributes of medical radiation protection sprays From National Medical Products Administration (NMPA) π¨π³ FGWJ-2022-148 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 29, 2022 Other (Public Domain) 0 reuses 0 favorites
Clarification of Radiation Control Regulations For Manufacturers of Diagnostic X-Ray Equipment: Draft Guidance for Industry and Food and Drug Administration Staff From Food and Drug Administration (FDA) πΊπΈ This document is a draft guidance for manufacturers of diagnostic X-ray equipment, providing clarification on radiation control regulations. Topics covered include export, import, and 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 April 26, 2021 Other (Public Domain) 0 reuses 0 favorites
Radiation Safety Considerations for X-Ray Equipment Designed for Hand-Held Use From Food and Drug Administration (FDA) πΊπΈ This document is a guidance on radiation safety for hand-held X-ray equipment, focusing on postmarket considerations. 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
Inspection and Field Testing of Radiation-Emitting Electronic Products: Attachment C: Specific Instructions for Sunlamp Product Inspections and Tests From Food and Drug Administration (FDA) πΊπΈ Guidance document providing specific instructions for inspections and tests of sunlamp products emitting radiation. 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
Clarification of Radiation Control Regulations for Diagnostic X-Ray Equipment (Part 3) From Food and Drug Administration (FDA) πΊπΈ Guidance document providing clarification on radiation control regulations for diagnostic X-ray equipment (Part 3). 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 2, 2020 Other (Public Domain) 0 reuses 0 favorites
Clarification of Radiation Control Regulations for Diagnostic X-Ray Equipment (Part 2) From Food and Drug Administration (FDA) πΊπΈ A memorandum providing clarification on radiation control regulations for diagnostic X-ray equipment. 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 2, 2020 Other (Public Domain) 0 reuses 0 favorites
Clarification of Radiation Control Regulations for Diagnostic X-Ray Equipment (Part 1 ) From Food and Drug Administration (FDA) πΊπΈ Guidance document providing clarification on radiation control regulations for diagnostic X-ray equipment (Part 1). 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 2, 2020 Other (Public Domain) 0 reuses 0 favorites
Radiation Biodosimetry Medical Countermeasure Devices: Guidance for Industry and Food and Drug Administration Staff From Food and Drug Administration (FDA) πΊπΈ This document provides guidance for the development and use of medical devices for radiation biodosimetry in emergencies. 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
Ordinance of 27 February 2019 to the Federal Act on Protection against the Risks associated with Non-Ionising Radiation and with Sound (O-NIRSA) From Swiss Federal Council π¨π The document is an ordinance titled "Ordinance of 27 February 2019 to the Federal Act on Protection against the Risks associated with Non-Ionising Radiation and with Sound (O-NIRSA)". 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 27, 2019 Other (Non-Commercial) 0 reuses 0 favorites
Clarification of Radiation Control Regulations for Diagnostic X-Ray Equipment (FDA 89-8221) From Food and Drug Administration (FDA) πΊπΈ Guidance document providing clarification on radiation control regulations for diagnostic X-ray equipment by FDA (89-8221). 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 9, 2019 Other (Public Domain) 0 reuses 0 favorites
Medical Devices; General Hospital and Personal Use Devices; Classification of the Ultraviolet Radiation Chamber Disinfection Device From Food and Drug Administration (FDA) πΊπΈ Document number 2015-29660. The Food and Drug Administration (FDA or the Agency) is classifying the ultraviolet (UV) radiation chamber disinfection device into class II (special controls). The special controls that will apply to the device are identified in this order and will be part of theβ¦ 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 20, 2015 Other (Public Domain) 0 reuses 0 favorites
Statement regarding Use of ISO 11137-1:2006 "Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices" From International Medical Device Regulators Forum (IMDRF) π Information document IMDRF/MC/N38 FINAL:2015. Metadata quality: Metadata quality: Data description empty Files documented 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 October 2, 2015 Other (Public Domain) 0 reuses 0 favorites
Resolution of the Collegiate Board of Directors - RDC No. 56 of 09/11/2009 From Brazilian Health Regulatory Agency (Anvisa) π§π· BANS THE USE OF ARTIFICIAL TANNING EQUIPMENT FOR AESTHETIC PURPOSES, BASED ON THE EMISSION OF ULTRAVIOLET RADIATION (UV). Metadata quality: Metadata quality: Data description filled Files documented 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: 66.66666666666666/100 Updated on November 9, 2009 Other (Public Domain) 0 reuses 0 favorites