Taiwan FDA registration 0247f9fa278f1d21a59acf6d9559fdf6
“JSM” Peripheral Guide Wire
TW: “吉生”周邊血管導引線
Taiwan·Risk Class 2·MD·JI SHENG MEDICAL COMPANY LIMITED·Registered Feb 26, 2014 – Feb 26, 2029ActiveRegistration details
- Analysis ID
- 0247f9fa278f1d21a59acf6d9559fdf6
- License Form
- Ministry of Health Medical Device Manufacturing No. 004536
Company information
- Manufacturer
- JI SHENG MEDICAL COMPANY LIMITED
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- JI SHENG MEDICAL COMPANY LIMITED
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)
- E1330 Catheter Lead
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Feb 26, 2014
- Expiry Date
- Feb 26, 2029
About this record
Access comprehensive regulatory information for “JSM” Peripheral Guide Wire in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0247f9fa278f1d21a59acf6d9559fdf6 and manufactured by JI SHENG MEDICAL COMPANY LIMITED. The authorized representative in Taiwan is JI SHENG MEDICAL COMPANY LIMITED.
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