中國

國家藥品監督管理局 www.nmpa.gov.cn

國家藥品監督管理局 數據查詢 http://app1.nmpa.gov.cn/data_nmpa/face3/dir.html?CbSlDlH0=qGcbkAr_8vN_8vN_8jp1szy7ruD4OwTMgq0JwJJKdoQqqoL

標準查詢 http://app.nifdc.org.cn/biaogzx/qxqwk.do

醫療器械行業標準 http://app.nifdc.org.cn/jianybz/jybzTwoGj.do?formAction=listTsDalid&type=ylqx&page=list_ylqx

醫療器械非采標推薦性行業標準http://app.nifdc.org.cn/jianybz/jybzTwoGj.do?formAction=listTsDalid&type=qxtjbz&page=list_qxtjbz

醫療器械分類目錄查詢http://app.nifdc.org.cn/biaogzx/dataGk.do

分類界定文件查詢http://app.nifdc.org.cn/biaogzx/flmlbczlk.do

I類產品補充分類信息http://app.nifdc.org.cn/biaogzx/flmlbczlk.do

醫療器械標準與分類管理https://www.nifdc.org.cn/nifdc/bshff/ylqxbzhgl/index.html

醫療器械法規查詢 https://www.nmpa.gov.cn/xxgk/fgwj/index.html

國家標準全文公開系統http://openstd.samr.gov.cn/bzgk/gb/index

分類目錄 指導原則 標準 https://www.cmde.org.cn/CL0195/

審評論壇 https://www.cmde.org.cn/CL0010/

器審云課堂 https://www.cmde.org.cn/CL0279/

國家局器審中心https://www.cmde.org.cn/CL0001/

醫療器械UDI數據庫 https://udi.nmpa.gov.cn/

醫療器械不良事件通報 https://www.nmpa.gov.cn/xxgk/yjjsh/ylqxblshjtb/index.html

醫療器械召回 https://www.nmpa.gov.cn/xxgk/chpzhh/ylqxzhh/index.html

國家局高級研修學院 http://nmpaied.org.cn/

國家醫療器械不良事件監測信息系統 https://maers.adrs.org.cn/console/login.ftl

國家局審核查驗中心 https://www.cfdi.org.cn/cfdi/index?module=A001&nty=A25

美國

美國FDA https://www.fda.gov/

美國聯邦法規https://www.ecfr.gov/cgi-bin/text-idx?SID=3ee286332416f26a91d9e6d786a604ab&mc=true&tpl=/ecfrbrowse/Title21/21tab_02.tpl

醫療器械數據庫 https://www.fda.gov/medical-devices/device-advice-comprehensive-regulatory-assistance/medical-device-databa[x]ses

CDRH Learn https://www.fda.gov/training-and-continuing-education/cdrh-learn

510K premarket notification https://www.accessdata.fda.gov/sc[x]ripts/cdrh/cfdocs/cfPMN/pmn.cfm

工廠注冊和器械列名 https://www.accessdata.fda.gov/sc[x]ripts/cdrh/cfdocs/cfRL/rl.cfm

產品分類數據庫 https://www.accessdata.fda.gov/sc[x]ripts/cdrh/cfdocs/cfpcd/classification.cfm

FDA認可標準數據庫 https://www.accessdata.fda.gov/sc[x]ripts/cdrh/cfdocs/cfStandards/search.cfm

審評指南數據庫 https://www.fda.gov/medical-devices/device-advice-comprehensive-regulatory-assistance/guidance-documents-medical-devices-and-radiation-emitting-products

FDA賬號注冊與登錄 https://www.access.fda.gov/oaa/logonFlow.htm?execution=e1s1

FDA自由信息法案https://www.fda.gov/regulatory-information/freedom-information

FDA法規簡介https://www.fda.gov/medical-devices/device-advice-comprehensive-regulatory-assistance

FDA UDI https://www.fda.gov/medical-devices/device-advice-comprehensive-regulatory-assistance/unique-device-identification-system-udi-system#ruleguidance

FDA MDSAP https://www.fda.gov/medical-devices/cdrh-international-programs/medical-device-single-audit-program-mdsap

MDR上報https://www.fda.gov/medical-devices/medical-device-safety/reporting-allegations-regulatory-misconduct

召回數據庫https://www.accessdata.fda.gov/sc[x]ripts/cdrh/cfdocs/cfRES/res.cfm

GUDID數據庫 https://accessgudid.nlm.nih.gov/

OSHA's Nationally Recognized Testing Laboratory (NRTL) https://www.osha.gov/nationally-recognized-testing-laboratory-program

歐盟

歐盟醫療器械信息 https://ec.europa.eu/health/md_sector/overview_en

歐盟醫療器械專家委員會 https://ec.europa.eu/health/md_expertpanels/overview_en

EUDAMED https://ec.europa.eu/health/md_eudamed/overview_en

EUDAMED數據庫https://webgate.ec.europa.eu/eudamed/landing-page#/

Medical Device Coordination Group Working Groups https://ec.europa.eu/health/md_dialogue/mdcg_working_groups_en

MDCG指南https://ec.europa.eu/health/md_sector/new_regulations/guidance_en#sec10

歐盟協調標準 https://ec.europa.eu/growth/single-market/european-standards/harmonised-standards_en

Basic UDI-DI生成 https://www.gs1.org/services/gmn-generator

公告機構Nando EUROPA - European Commission - Growth - Regulatory policy - NANDO