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Kunxia immunoglobulin test set - Taiwan Registration 8b1097e3828330afb208bd5458a73054

Access comprehensive regulatory information for Kunxia immunoglobulin 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 8b1097e3828330afb208bd5458a73054 and manufactured by BIOKIT, S.A.. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).

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8b1097e3828330afb208bd5458a73054
Registration Details
Taiwan FDA Registration: 8b1097e3828330afb208bd5458a73054
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Device Details

Kunxia immunoglobulin test set
TW: ๆ˜†ๅ–œไบžๅ…็–ซ็ƒ่›‹็™ฝๆชข้ฉ—่ฉฆๅŠ‘็ต„
Risk Class 2

Registration Details

8b1097e3828330afb208bd5458a73054

DHA00602309600

Company Information

Product Details

This product is used with the ARCHITECT c system to quantitatively test immunoglobulin E (IgE) in human serum or plasma.

A Clinical chemistry and clinical toxicology

A.1150 Calibrated Products

import

Dates and Status

Jan 30, 2012

Jan 30, 2027