Pure Global
Taiwan FDA registration 548a0cbe727347c50d408e5b9ef2aa34

"St. Yoda" Clenterplath implantable heart rhythm defibrillator

TW: “聖猷達”克侖特普拉斯植入式心律去顫器
Taiwan flagTaiwan·Risk Class 3·ST. JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Registered May 29, 2012 – May 29, 2022Cancelled
Registration details
Analysis ID
548a0cbe727347c50d408e5b9ef2aa34
Customs Code
DHA00602351701
Company information
Manufacturer
ST. JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION
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
May 29, 2012
Expiry Date
May 29, 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. Yoda" Clenterplath 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 548a0cbe727347c50d408e5b9ef2aa34 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