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Kunxia β2-microglobulin assay set - Taiwan Registration 16ae2dd32d4161b91ce9e05e185e42d1

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.

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16ae2dd32d4161b91ce9e05e185e42d1
Registration Details
Taiwan FDA Registration: 16ae2dd32d4161b91ce9e05e185e42d1
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Device Details

Kunxia β2-microglobulin assay set
TW: 昆喜亞β2-微球蛋白檢驗試劑組
Risk Class 2

Registration Details

16ae2dd32d4161b91ce9e05e185e42d1

DHA05602681106

Company Information

Product Details

This product can be used with the ARCHITECT c System to quantitatively test β2-microglobulin (β2M) in serum, plasma (EDTA) or urine.

C Immunology and Microbiology; A Clinical chemistry and clinical toxicology

C.5630 β-2-微球蛋白免疫試驗系統;; A.1150 校正品

import

Dates and Status

Dec 09, 2014

Dec 09, 2029