Taiwan FDA registration c624aa22b910e98044b44f163dd5bdfe
"Keithley" Kant dual-chamber synchronous rectifier/defibrillator
TW: "吉時利" 康德雙腔同步整律/去顫器
Taiwan·GUIDANT IRELAND·Registered Mar 23, 2005 – Apr 21, 2010CancelledRegistration details
- Analysis ID
- c624aa22b910e98044b44f163dd5bdfe
- Customs Code
- DHA00601111807
Company information
- Manufacturer
- GUIDANT IRELAND
- Manufacturer Country
- Ireland
- Authorized Representative
- Xiongqun Enterprise Limited
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
- import
Dates and status
- Registration Date
- Mar 23, 2005
- Expiry Date
- Apr 21, 2010
- Cancellation Date
- Oct 26, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Keithley" Kant dual-chamber synchronous rectifier/defibrillator in Taiwan's medical device market through Pure Global AI's free database. is registered under number c624aa22b910e98044b44f163dd5bdfe and manufactured by GUIDANT IRELAND. The authorized representative in Taiwan is Xiongqun Enterprise Limited.
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