Taiwan FDA registration 16ae2dd32d4161b91ce9e05e185e42d1
Kunxia β2-microglobulin assay set
TW: 昆喜亞β2-微球蛋白檢驗試劑組
Taiwan·Risk Class 2·BIOKIT, S.A.·Registered Dec 09, 2014 – Dec 09, 2029ActiveRegistration details
- Analysis ID
- 16ae2dd32d4161b91ce9e05e185e42d1
- Customs Code
- DHA05602681106
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 can be used with the ARCHITECT c System to quantitatively test β2-microglobulin (β2M) in serum, plasma (EDTA) or urine.
- Product Type (Level 1)
- C Immunology and Microbiology; A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- C.5630 β-2-微球蛋白免疫試驗系統;; A.1150 校正品
- Import Information
- import
Dates and status
- Registration Date
- Dec 09, 2014
- Expiry Date
- Dec 09, 2029
About this record
Access comprehensive regulatory information for Kunxia β2-microglobulin assay set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 16ae2dd32d4161b91ce9e05e185e42d1 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