Taiwan FDA registration e058f94aed47ffbaeb55c5ee0b7003f6
Kunxia Rheumatoid Factor Test Set
TW: 昆喜亞類風濕因子檢驗試劑組
Registration details
- Analysis ID
- e058f94aed47ffbaeb55c5ee0b7003f6
- Customs Code
- DHA05602553006
Company information
- Manufacturer
- BIOKIT, S.A.
- Manufacturer Country
- Spain
- Authorized Representative
- ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.)
Product details
- Intended Use
- This product is used in conjunction with ARCHITECT cSystems to quantitatively detect rheumatoid factors (RF) in human serum.
- Product Type (Level 1)
- C Immunology and Microbiology; A Clinical chemistry and clinical toxicology
- 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
- Oct 18, 2013
- Expiry Date
- Oct 18, 2028
About this record
Access comprehensive regulatory information for Kunxia Rheumatoid Factor Test Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e058f94aed47ffbaeb55c5ee0b7003f6 and manufactured by BIOKIT, S.A.. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).
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