Taiwan FDA registration df655c413499f8f15121f50b80e3fb8b
“MicroPort” EasyFinder Diagnostic Catheter
TW: “微創電生理”診斷導管
Taiwan·Risk Class 2·MD·SHANGHAI MICROPORT EP MEDTECH CO, LTD.·Registered Apr 22, 2018 – Apr 22, 2023ExpiredRegistration details
- Analysis ID
- df655c413499f8f15121f50b80e3fb8b
- License Form
- Ministry of Health Medical Device Land Transport No. 000900
- Customs Code
- DHA09200090006
Company information
- Manufacturer
- SHANGHAI MICROPORT EP MEDTECH CO, LTD.
- Manufacturer Country
- China
- Authorized Representative
- IDS MEDICAL SYSTEMS (HONG KONG) COMPANY LIMITED, TAIWAN BRANCH (HONG KONG)
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E1220 electrode recording catheter or electrode recording probe
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 22, 2018
- Expiry Date
- Apr 22, 2023
About this record
Access comprehensive regulatory information for “MicroPort” EasyFinder Diagnostic Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number df655c413499f8f15121f50b80e3fb8b and manufactured by SHANGHAI MICROPORT EP MEDTECH CO, LTD.. The authorized representative in Taiwan is IDS MEDICAL SYSTEMS (HONG KONG) COMPANY LIMITED, TAIWAN BRANCH (HONG KONG).
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