Taiwan FDA registration 51a29d87ae0aab7a7b1a6a7f7c18eff6
"Shengyoda" through the middle diaphragm duct system
TW: “聖猷達”經中膈導管系統
Taiwan·Risk Class 2·ST. JUDE MEDICAL·Registered Jul 09, 2008 – Jul 09, 2018CancelledRegistration details
- Analysis ID
- 51a29d87ae0aab7a7b1a6a7f7c18eff6
- Customs Code
- DHA00601909904
Company information
- Manufacturer
- ST. JUDE MEDICAL
- Manufacturer Country
- United States
- Authorized Representative
- Taiwan Shengyuda Medical Supplies Co., Ltd
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 導管導引器;; E.1390 套管針
- Import Information
- import
Dates and status
- Registration Date
- Jul 09, 2008
- Expiry Date
- Jul 09, 2018
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Shengyoda" through the middle diaphragm duct system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 51a29d87ae0aab7a7b1a6a7f7c18eff6 and manufactured by ST. JUDE MEDICAL. The authorized representative in Taiwan is Taiwan Shengyuda Medical Supplies Co., Ltd.
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