Taiwan FDA registration cb9af4e714ff815765f3caf3123f1892
"Otto" atrial septal complementer
TW: “奧圖”心房中隔補綴器
Taiwan·Risk Class 3·OCCLUTECH GMBH·Registered Apr 13, 2011 – Apr 13, 2016CancelledRegistration details
- Analysis ID
- cb9af4e714ff815765f3caf3123f1892
- Customs Code
- DHA00602226801
Company information
- Manufacturer
- OCCLUTECH GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- WATTCAN INSTRUMENTS CO., LTD.
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
- Apr 13, 2011
- Expiry Date
- Apr 13, 2016
- Cancellation Date
- Jun 26, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Otto" atrial septal complementer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number cb9af4e714ff815765f3caf3123f1892 and manufactured by OCCLUTECH GMBH. The authorized representative in Taiwan is WATTCAN INSTRUMENTS CO., LTD..
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