Taiwan FDA registration dc091c3fb30acf4d2d4256ada8204d0e
“Siemens” Estradiol Control
TW: “西門子” 雌二醇品管液
Taiwan·Risk Class 2·MD·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LIMITED·Registered Oct 22, 2013 – Oct 22, 2018CancelledRegistration details
- Analysis ID
- dc091c3fb30acf4d2d4256ada8204d0e
- License Form
- Ministry of Health Medical Device Import No. 025532
- Customs Code
- DHA05602553200
Company information
- Manufacturer
- SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LIMITED
- Manufacturer Country
- United Kingdom
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
Product details
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1660 Quality Control Materials (Analytical and Non-Analytical)
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 22, 2013
- Expiry Date
- Oct 22, 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 “Siemens” Estradiol Control in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dc091c3fb30acf4d2d4256ada8204d0e and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LIMITED. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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