Taiwan FDA registration fea98b1ecb87cc4e39d24128da4b197b
"Yoshisen" cardiac catheterization package
TW: “吉生”心導管包
Taiwan·Risk Class 2·JI SHENG MEDICAL COMPANY LIMITED·Registered Jan 10, 2012 – Jan 10, 2027ActiveRegistration details
- Analysis ID
- fea98b1ecb87cc4e39d24128da4b197b
- Customs Code
- DHY00500352201
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 Medicine Science
- Product Type (Level 2)
- E.1340 Catheter Introducers
- Import Information
- Domestic
Dates and status
- Registration Date
- Jan 10, 2012
- Expiry Date
- Jan 10, 2027
About this record
Access comprehensive regulatory information for "Yoshisen" cardiac catheterization package in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fea98b1ecb87cc4e39d24128da4b197b and manufactured by JI SHENG MEDICAL COMPANY LIMITED. The authorized representative in Taiwan is JI SHENG MEDICAL COMPANY LIMITED.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices