Taiwan FDA registration 4d0aa13b418936ebd70c7691eec7d791
Konya liquid immunoassay solution
TW: 科尼亞液狀免疫品管液
Taiwan·Risk Class 2·KAMIYA BIOMEDICAL COMPANY·Registered Aug 04, 2006 – Aug 04, 2021CancelledRegistration details
- Analysis ID
- 4d0aa13b418936ebd70c7691eec7d791
- Customs Code
- DHA00601726103
Company information
- Manufacturer
- KAMIYA BIOMEDICAL COMPANY
- Manufacturer Country
- United States
- Authorized Representative
- TUNYEN ENTERPRISE CORPORATION
Product details
- Intended Use
- 作為已知濃度之檢體,監控免疫比濁定量分析法(immunoturbidimetric assay)之效能.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1660 Quality control materials (analytical and non-analytical)
- Import Information
- import
Dates and status
- Registration Date
- Aug 04, 2006
- Expiry Date
- Aug 04, 2021
- Cancellation Date
- Jul 08, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for Konya liquid immunoassay solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4d0aa13b418936ebd70c7691eec7d791 and manufactured by KAMIYA BIOMEDICAL COMPANY. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.
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