Taiwan FDA registration b1cb0fcb448c14d7f8083c438610e7a4
"St. Yoda" defibrillation electrocatheter
TW: “聖猷達” 除顫電燒導管
Taiwan·Risk Class 3·ST. JUDE MEDICAL·Registered Oct 16, 2013 – Oct 16, 2028ActiveRegistration details
- Analysis ID
- b1cb0fcb448c14d7f8083c438610e7a4
- Customs Code
- DHA05602543502
Company information
- Manufacturer
- ST. JUDE MEDICAL
- 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.0008.
- Import Information
- import
Dates and status
- Registration Date
- Oct 16, 2013
- Expiry Date
- Oct 16, 2028
About this record
Access comprehensive regulatory information for "St. Yoda" defibrillation electrocatheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number b1cb0fcb448c14d7f8083c438610e7a4 and manufactured by ST. JUDE MEDICAL. The authorized representative in Taiwan is Abbott Medical Taiwan Co..
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