Taiwan FDA registration aca28e2636461bece78d2f3989fd76d3
Cell cryogenic equipment and reactants for in vitro diagnosis of "Jide"
TW: “吉得”體外診斷用的細胞冷凍設備及反應劑
Taiwan·Risk Class 1·ZELTIQ AESTHETICS, INC.·Registered Oct 28, 2010 – Oct 28, 2015CancelledRegistration details
- Analysis ID
- aca28e2636461bece78d2f3989fd76d3
- Customs Code
- DHA04400942301
Company information
- Manufacturer
- ZELTIQ AESTHETICS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- SHAWHAN BIOMEDICAL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of cell cryogenic equipment and reactants (B.9225) for in vitro diagnosis of medical device management methods.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.9225 Cell freezing equipment and reagents for in vitro diagnostics
- Import Information
- import
Dates and status
- Registration Date
- Oct 28, 2010
- Expiry Date
- Oct 28, 2015
- Cancellation Date
- May 28, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Cell cryogenic equipment and reactants for in vitro diagnosis of "Jide" in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number aca28e2636461bece78d2f3989fd76d3 and manufactured by ZELTIQ AESTHETICS, INC.. The authorized representative in Taiwan is SHAWHAN BIOMEDICAL CO., LTD..
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