Taiwan FDA registration a016f82ffd4e027f345db909035132ee
Konya ferritin reagent
TW: 科尼亞運鐵蛋白試劑
Taiwan·Risk Class 2·KAMIYA BIOMEDICAL COMPANY·Registered Aug 09, 2006 – Aug 09, 2021CancelledRegistration details
- Analysis ID
- a016f82ffd4e027f345db909035132ee
- Customs Code
- DHA00601726600
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)定量測定人類血清中運鐵蛋白(Transferrin).
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.5880 運鐵蛋白免疫試驗系統
- 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 ferritin reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a016f82ffd4e027f345db909035132ee and manufactured by KAMIYA BIOMEDICAL COMPANY. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices