Taiwan FDA registration a5d851dde30df06b5e8af778dbeed592
"Hao Kensheng" vascular diagnostic instrument
TW: "好肯生" 血管診斷儀
Taiwan·Risk Class 2·D.E. HOKANSON INC.·Registered Sep 13, 2005 – Sep 13, 2015CancelledRegistration details
- Analysis ID
- a5d851dde30df06b5e8af778dbeed592
- Customs Code
- DHA00601191303
Company information
- Manufacturer
- D.E. HOKANSON INC.
- Manufacturer Country
- United States
- Authorized Representative
- NIEN TAI MEDICAL 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
- Sep 13, 2005
- Expiry Date
- Sep 13, 2015
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Hao Kensheng" vascular diagnostic instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a5d851dde30df06b5e8af778dbeed592 and manufactured by D.E. HOKANSON INC.. The authorized representative in Taiwan is NIEN TAI MEDICAL INSTRUMENTS CO., LTD..
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