Taiwan FDA registration 865973f5218fffe82e2b2e4ef3a2b176
“JSM” Insertion Kit
TW: “吉生”穿刺套組
Taiwan·Risk Class 2·MD·JI SHENG MEDICAL COMPANY LIMITED·Registered Jun 26, 2014 – Jun 26, 2024ExpiredRegistration details
- Analysis ID
- 865973f5218fffe82e2b2e4ef3a2b176
- License Form
- Ministry of Health Medical Device Manufacturing No. 004631
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)
- E1340 Catheter Guide
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Jun 26, 2014
- Expiry Date
- Jun 26, 2024
About this record
Access comprehensive regulatory information for “JSM” Insertion Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 865973f5218fffe82e2b2e4ef3a2b176 and manufactured by JI SHENG MEDICAL COMPANY LIMITED. The authorized representative in Taiwan is JI SHENG MEDICAL COMPANY LIMITED.
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