Taiwan FDA registration d52fa647698dcc067451b8d4038a092d
"Berlin Heart" mobile drive for Aesker ventricular assist device
TW: “柏林心臟”艾斯科心室輔助裝置用移動式驅動器
Taiwan·Risk Class 3·BERLIN HEART GMBH·Registered Aug 05, 2009 – Aug 05, 2019CancelledRegistration details
- Analysis ID
- d52fa647698dcc067451b8d4038a092d
- Customs Code
- DHA00602035904
Company information
- Manufacturer
- BERLIN HEART GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- ANSON HEALTH CARE INC.
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.3545 心室血管繞道術(輔助)裝置
- Import Information
- import
Dates and status
- Registration Date
- Aug 05, 2009
- Expiry Date
- Aug 05, 2019
- Cancellation Date
- May 19, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Berlin Heart" mobile drive for Aesker ventricular assist device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number d52fa647698dcc067451b8d4038a092d and manufactured by BERLIN HEART GMBH. The authorized representative in Taiwan is ANSON HEALTH CARE INC..
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