Taiwan FDA registration 98cbbb2e8c8ac7a2b1ef051f6ffeabdd
"St. Yoda" Katikais Electric cautery catheter
TW: “聖猷達”卡帝凱斯 電燒導管
Registration details
- Analysis ID
- 98cbbb2e8c8ac7a2b1ef051f6ffeabdd
- Customs Code
- DHA05602785607
Company information
- Manufacturer Country
- Mexico;;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
- Import Information
- Contract manufacturing;; input
Dates and status
- Registration Date
- Nov 24, 2015
- Expiry Date
- Nov 24, 2025
About this record
Access comprehensive regulatory information for "St. Yoda" Katikais Electric cautery catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 98cbbb2e8c8ac7a2b1ef051f6ffeabdd and manufactured by St. Jude Medical; Venusa de México S. de R.L. de C.V.. 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