Taiwan FDA registration ed6c77884a374430957754d2490cc310
Konya multi-analytical calibration solution
TW: 科尼亞多項分析校正液
Taiwan·Risk Class 2·KAMIYA BIOMEDICAL COMPANY·Registered Aug 09, 2006 – Aug 09, 2021CancelledRegistration details
- Analysis ID
- ed6c77884a374430957754d2490cc310
- Customs Code
- DHA00601726501
Company information
- Manufacturer
- KAMIYA BIOMEDICAL COMPANY
- Manufacturer Country
- United States
- Authorized Representative
- TUNYEN ENTERPRISE CORPORATION
Product details
- Intended Use
- 此K-ASSAY®多項分析校正液主要為α-1 AG,α-1 AT, C3, C4, Haptoglobin, IgA, IgG, IgM, 及 Transferrin. 利用免疫比濁法定量測定(immunoturbidimetric assay)時所需之校正液.
- 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 09, 2006
- Expiry Date
- Aug 09, 2021
- Cancellation Date
- Jun 29, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for Konya multi-analytical calibration solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ed6c77884a374430957754d2490cc310 and manufactured by KAMIYA BIOMEDICAL COMPANY. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.
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