Speedodine RA test reagent - Taiwan Registration ab29595812690bb555029de513182041
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.
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.
Device Details
Product Details
ๅฉ็จ่ขซๅ็ฒๅญๅ้ๆณๆชขๆธฌไบบ่กๆธ ไธญไนRheumatoid Factor.
C Immunology and microbiology
C.5775 ้ก้ขจๆฟๆงๅ ๅญๅ ็ซ่ฉฆ้ฉ็ณป็ตฑ
import
Dates and Status
Dec 13, 2005
Dec 13, 2015
May 17, 2018
Cancellation Information
Logged out
่จฑๅฏ่ญๅทฒ้พๆๆๆ

