Taiwan FDA registration fc3282711671cb9466c20d93afcf0304
"Medtronic" subthoracic extrapericardial ECG scanning device
TW: 〝美敦力〞胸下心包外心電掃描裝置
Taiwan·Risk Class 1·MEDTRONIC PERFUSION SYSTEMS·Registered Oct 17, 2005 – Oct 17, 2010CancelledRegistration details
- Analysis ID
- fc3282711671cb9466c20d93afcf0304
- Customs Code
- DHA04400097600
Company information
- Manufacturer
- MEDTRONIC PERFUSION SYSTEMS
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- It is used to direct fluid from the pericardium or chest cavity.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Import Information
- import
Dates and status
- Registration Date
- Oct 17, 2005
- Expiry Date
- Oct 17, 2010
- Cancellation Date
- Nov 06, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Medtronic" subthoracic extrapericardial ECG scanning device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fc3282711671cb9466c20d93afcf0304 and manufactured by MEDTRONIC PERFUSION SYSTEMS. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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