Taiwan FDA registration f316d8c2047b8e344091ab17a5c4c25a
and photorheumatoid factor immunoreagents
TW: 和光類風濕性因子免疫試劑
Taiwan·Risk Class 2·FUJIFILM WAKO PURE CHEMICAL CORPORATION MIE PLANT·Registered Jun 11, 2009 – Jun 11, 2029ActiveRegistration details
- Analysis ID
- f316d8c2047b8e344091ab17a5c4c25a
- Customs Code
- DHA00602033302
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- MEDICARE PRODUCTS INC.
Product details
- Intended Use
- It is used to quantitatively determine the activity of rheumatic factors such as serum or plasma.
- Product Type (Level 1)
- A Clinical Chemistry and Clinical Toxicology;; C Immunology and Microbiology
- Product Type (Level 2)
- C.5775 類風濕性因子免疫試驗系統;; A.1150 校正品
- Import Information
- import
Dates and status
- Registration Date
- Jun 11, 2009
- Expiry Date
- Jun 11, 2029
About this record
Access comprehensive regulatory information for and photorheumatoid factor immunoreagents in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f316d8c2047b8e344091ab17a5c4c25a and manufactured by FUJIFILM WAKO PURE CHEMICAL CORPORATION MIE PLANT. The authorized representative in Taiwan is MEDICARE PRODUCTS INC..
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