Taiwan FDA registration 49f0bdb2632ebf96a2535e8cecb9837c
“ESTECH” Cobra Revolution Bipolar Clamp
TW: “艾斯泰格”康柏拉雙極電燒鉗
Taiwan·Risk Class 2·MD·ENDOSCOPIC TECHNOLOGIES, INC. DBA: ESTECH·Registered Jul 27, 2013 – Jul 27, 2018CancelledRegistration details
- Analysis ID
- 49f0bdb2632ebf96a2535e8cecb9837c
- License Form
- Ministry of Health Medical Device Import No. 025306
- Customs Code
- DHA05602530601
Company information
- Manufacturer
- ENDOSCOPIC TECHNOLOGIES, INC. DBA: ESTECH
- Manufacturer Country
- United States
- Authorized Representative
- ASIA HEALTH CARE CO., LTD.
Product details
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4400 Electric knife for cutting and hemostasis and its accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 27, 2013
- Expiry Date
- Jul 27, 2018
- Cancellation Date
- May 19, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證逾有效期未申請展延
About this record
Access comprehensive regulatory information for “ESTECH” Cobra Revolution Bipolar Clamp in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 49f0bdb2632ebf96a2535e8cecb9837c and manufactured by ENDOSCOPIC TECHNOLOGIES, INC. DBA: ESTECH. The authorized representative in Taiwan is ASIA HEALTH CARE CO., LTD..
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