Taiwan FDA registration 69499f1036de7c46e4f8859cad6e333d
Konya microalbumin urine reagent
TW: 科尼亞微量白蛋白尿液試劑
Taiwan·Risk Class 2·KAMIYA BIOMEDICAL COMPANY·Registered Oct 01, 2007 – Oct 01, 2022CancelledRegistration details
- Analysis ID
- 69499f1036de7c46e4f8859cad6e333d
- Customs Code
- DHA00601843706
Company information
- Manufacturer
- KAMIYA BIOMEDICAL COMPANY
- Manufacturer Country
- United States
- Authorized Representative
- TUNYEN ENTERPRISE CORPORATION
Product details
- Intended Use
- 利用免疫比濁法(immunoturbidimetric assay) 定量測定人類尿液中微量白蛋白 (Microalbumin),此試劑僅適用於體外診斷.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.5040 白蛋白免疫試驗系統
- Import Information
- import
Dates and status
- Registration Date
- Oct 01, 2007
- Expiry Date
- Oct 01, 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 microalbumin urine reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 69499f1036de7c46e4f8859cad6e333d and manufactured by KAMIYA BIOMEDICAL COMPANY. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.
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