Taiwan FDA registration 85f54c197e16fe90166313c79f144f51
"Estellar" intravenous catheter
TW: “艾斯泰格”靜脈導管
Taiwan·Risk Class 2·ENDOSCOPIC TECHNOLOGIES, INC.·Registered Dec 23, 2009 – Dec 23, 2014CancelledRegistration details
- Analysis ID
- 85f54c197e16fe90166313c79f144f51
- Customs Code
- DHA00602051008
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)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.4210 Vascular catheters, cannulas and tubes for cardiopulmonary vascular bypassing
- Import Information
- import
Dates and status
- Registration Date
- Dec 23, 2009
- Expiry Date
- Dec 23, 2014
- Cancellation Date
- Jul 31, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Estellar" intravenous catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 85f54c197e16fe90166313c79f144f51 and manufactured by ENDOSCOPIC TECHNOLOGIES, INC.. The authorized representative in Taiwan is ASIA HEALTH CARE CO., LTD..
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