Taiwan FDA registration 42d8e1e99eb358566f0f50eab8b6e44f
"Jisheng" extracorporeal bypass tube group
TW: “吉生”體外循環管組
Taiwan·Risk Class 2·JI SHENG MEDICAL COMPANY LIMITED·Registered Mar 28, 2013 – Mar 28, 2028ActiveRegistration details
- Analysis ID
- 42d8e1e99eb358566f0f50eab8b6e44f
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.4360 非滾筒式心肺血管繞道術血液循環幫浦
- Import Information
- Domestic
Dates and status
- Registration Date
- Mar 28, 2013
- Expiry Date
- Mar 28, 2028
About this record
Access comprehensive regulatory information for "Jisheng" extracorporeal bypass tube group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 42d8e1e99eb358566f0f50eab8b6e44f and manufactured by JI SHENG MEDICAL COMPANY LIMITED. The authorized representative in Taiwan is JI SHENG MEDICAL COMPANY LIMITED.
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