Taiwan FDA registration 30b1975db66cbb34b3f5d652ae523bad
"St. Yoda" inner catheter
TW: “聖猷達”內導管
Taiwan·Risk Class 2·St. Jude Medical, Cardiac Rhythm Management Division·Registered Sep 07, 2007 – Sep 07, 2017CancelledRegistration details
- Analysis ID
- 30b1975db66cbb34b3f5d652ae523bad
- Customs Code
- DHA00601831202
Company information
- 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.1250 Percutaneous catheters
- Import Information
- import
Dates and status
- Registration Date
- Sep 07, 2007
- Expiry Date
- Sep 07, 2017
- Cancellation Date
- Nov 04, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "St. Yoda" inner catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 30b1975db66cbb34b3f5d652ae523bad and manufactured by St. Jude Medical, Cardiac Rhythm Management Division. The authorized representative in Taiwan is Taiwan Shengyuda Medical Supplies Co., Ltd.
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