Taiwan FDA registration ab29595812690bb555029de513182041
Speedodine RA test reagent
TW: 速樂定RA檢驗試劑
Taiwan·Risk Class 2·FUJIREBIO INC., HACHIOJI FACILITY·Registered Dec 13, 2005 – Dec 13, 2015CancelledRegistration details
- Analysis ID
- ab29595812690bb555029de513182041
- Customs Code
- DHA00601550801
Company information
- Manufacturer
- FUJIREBIO INC., HACHIOJI FACILITY
- Manufacturer Country
- Japan
- Authorized Representative
- Taiwan Fu Pharmaceutical Co., Ltd
Product details
- Intended Use
- 利用被動粒子凝集法檢測人血清中之Rheumatoid Factor.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.5775 類風濕性因子免疫試驗系統
- Import Information
- import
Dates and status
- Registration Date
- Dec 13, 2005
- Expiry Date
- Dec 13, 2015
- Cancellation Date
- May 17, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Speedodine RA test reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ab29595812690bb555029de513182041 and manufactured by FUJIREBIO INC., HACHIOJI FACILITY. The authorized representative in Taiwan is Taiwan Fu Pharmaceutical Co., Ltd.
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