Taiwan FDA registration 715afaa9b9ac13a50a92dac15cc566fd
"Estelle" Compalla bipolar sleeve
TW: “艾斯泰格”康柏拉電雙極套
Taiwan·Risk Class 2·ENDOSCOPIC TECHNOLOGIES, INC.·Registered May 09, 2007 – May 09, 2017CancelledRegistration details
- Analysis ID
- 715afaa9b9ac13a50a92dac15cc566fd
- Customs Code
- DHA00601807001
Company information
- Manufacturer
- ENDOSCOPIC TECHNOLOGIES, INC.
- Manufacturer Country
- United States
- Authorized Representative
- ASIA HEALTH CARE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4400 Cutting and hemostasis electric knives and accessories thereof
- Import Information
- import
Dates and status
- Registration Date
- May 09, 2007
- Expiry Date
- May 09, 2017
- Cancellation Date
- Nov 18, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Estelle" Compalla bipolar sleeve in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 715afaa9b9ac13a50a92dac15cc566fd and manufactured by ENDOSCOPIC TECHNOLOGIES, INC.. The authorized representative in Taiwan is ASIA HEALTH CARE CO., LTD..
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