印度医疗器械监管概述
Outline of India Medical Device Supervision
8防污公约附则I强制报告制度格式
Form of Mandatory Reporting System of Annex I of MARPOL 7378 737
进度报告制度
progress reporting system
德国医疗器械行业近况
Recent of Medical Devices Industry in Germany
非植入医疗器械
non-implanting medical device
高风险医疗器械
high-risk medical equipment
关注我国医疗器械工业
Focus on the Medical Equipment Industry
韩国医疗器械监管概述
The Supervision of Medical Device in Korea
合作医疗制度
cooperative medical system
cooperative medical policy
Cooperative medical scheme
家庭医疗器械
household medical appliance
进口医疗器械
import medical instrument
可降解一次性使用医疗器械
Degradable Single-use Medical Apparatus
可疑医疗器械不良事件
suspected medical device adverse event
可疑医疗器械不良事件报告表
adverse events of medical device reports
口腔医疗器械
Oral cavity medical apparatus
跨国医疗器械企业
multinational medical equipment manufacturers