Taiwan FDA registration 172722e13267c1f636402c76ca35df68
"San Youda" Krzo Azola multi-point implantable cardiac rhythm defibrillator
TW: “聖猷達”克卓亞速拉多點式植入式心律去顫器
Taiwan·Risk Class 3·St. Jude Medical, Cardiac Rhythm Management Division·Registered Feb 07, 2013 – Feb 07, 2023ExpiredRegistration details
- Analysis ID
- 172722e13267c1f636402c76ca35df68
- Customs Code
- DHA00602441508
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
- Feb 07, 2013
- Expiry Date
- Feb 07, 2023
About this record
Access comprehensive regulatory information for "San Youda" Krzo Azola multi-point implantable cardiac 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 172722e13267c1f636402c76ca35df68 and manufactured by St. Jude Medical, Cardiac Rhythm Management Division. The authorized representative in Taiwan is Abbott Medical Taiwan Co..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices