Taiwan FDA registration c4ee31778ac1b6eaae045efb72ff1a6a
"Estelle" Cumbera surgical adsorption system
TW: “艾斯泰格”康柏拉外科吸附系統
Taiwan·Risk Class 2·ENDOSCOPIC TECHNOLOGIES, INC.·Registered Jun 26, 2007 – Jun 26, 2012CancelledRegistration details
- Analysis ID
- c4ee31778ac1b6eaae045efb72ff1a6a
- Customs Code
- DHA00601814009
Company information
- Manufacturer
- ENDOSCOPIC TECHNOLOGIES, INC.
- Manufacturer Country
- United States
- Authorized Representative
- ASIA HEALTH CARE CO., LTD.
Product details
- Intended Use
- Details are as follows: the approved version of the Chinese interview form.
- 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
- Jun 26, 2007
- Expiry Date
- Jun 26, 2012
- Cancellation Date
- Jul 25, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Estelle" Cumbera surgical adsorption system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c4ee31778ac1b6eaae045efb72ff1a6a and manufactured by ENDOSCOPIC TECHNOLOGIES, INC.. The authorized representative in Taiwan is ASIA HEALTH CARE CO., LTD..
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