Taiwan FDA registration f331cad1d7c4b6f8fd73639de5a2a94f
"St. Uda" Fertima Azola implantable heart rhythm defibrillator
TW: “聖猷達”弗帝法亞速拉植入式心律去顫器
Taiwan·Risk Class 3·St. Jude Medical, Cardiac Rhythm Management Division·Registered Nov 20, 2012 – Nov 20, 2022CancelledRegistration details
- Analysis ID
- f331cad1d7c4b6f8fd73639de5a2a94f
- Customs Code
- DHA00602417300
Company information
- Manufacturer Country
- United States
- Authorized Representative
- Abbott Medical Taiwan Co.
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.3610 Pulsator of implantable cardiac rhythm apparatus
- Import Information
- import
Dates and status
- Registration Date
- Nov 20, 2012
- Expiry Date
- Nov 20, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "St. Uda" Fertima Azola implantable heart rhythm defibrillator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number f331cad1d7c4b6f8fd73639de5a2a94f and manufactured by St. Jude Medical, Cardiac Rhythm Management Division. The authorized representative in Taiwan is Abbott Medical Taiwan Co..
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