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Optilite Freelite Mx Lambda Free Kit - Taiwan Registration d880fbe1977fb47c64a07bd79ebfafce

Access comprehensive regulatory information for Optilite Freelite Mx Lambda Free Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d880fbe1977fb47c64a07bd79ebfafce and manufactured by THE BINDING SITE GROUP LTD. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) CO., LTD..

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d880fbe1977fb47c64a07bd79ebfafce
Registration Details
Taiwan FDA Registration: d880fbe1977fb47c64a07bd79ebfafce
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Device Details

Optilite Freelite Mx Lambda Free Kit
TW: ๆญๆ™ฎ็พ…่‡ช็”ฑ่ผ•้ˆ็ฑณๅ…‹ๆ–ฏไบบ้กžๅ€ซ้”่ฉฆๅŠ‘ๅฅ—็ต„
Risk Class 2
MD

Registration Details

d880fbe1977fb47c64a07bd79ebfafce

Ministry of Health Medical Device Import No. 032144

DHA05603214405

Company Information

United Kingdom

Product Details

This product is an in vitro diagnostic reagent with "Taiyang" Opro optimized protein analysis system for the quantitative determination of lambda free light chain in vitro, suitable for plasma, urine or CSF (cerebrospinal fluid) with serum, heparin lithium salt and EDTA as anticoagulants.

C Immunology and microbiology devices

C5550 Immunoglobulin (Specific Light Chain) Immunoassay System

Imported from abroad

Dates and Status

Jan 24, 2019

Jan 24, 2029