Taiwan FDA registration 0e7bbe1d11e77442f642294151db9367
Konya proprotein correction solution
TW: 科尼亞前蛋白校正液
Taiwan·Risk Class 2·KAMIYA BIOMEDICAL COMPANY·Registered Aug 21, 2007 – Aug 21, 2022CancelledRegistration details
- Analysis ID
- 0e7bbe1d11e77442f642294151db9367
- Customs Code
- DHA00601841904
Company information
- Manufacturer
- KAMIYA BIOMEDICAL COMPANY
- Manufacturer Country
- United States
- Authorized Representative
- TUNYEN ENTERPRISE CORPORATION
Product details
- Intended Use
- The calibration solution required for the quantification of prealbumin by immunoturbidimetry.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1150 Calibrated Products
- Import Information
- import
Dates and status
- Registration Date
- Aug 21, 2007
- Expiry Date
- Aug 21, 2022
- Cancellation Date
- Jun 29, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for Konya proprotein correction solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0e7bbe1d11e77442f642294151db9367 and manufactured by KAMIYA BIOMEDICAL COMPANY. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.
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