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"Randox" Lithium 2 - Taiwan Registration ec0633c12b44b5f06c0807848e9dbc0e

Access comprehensive regulatory information for "Randox" Lithium 2 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ec0633c12b44b5f06c0807848e9dbc0e and manufactured by RANDOX LABORATORIES LTD.. The authorized representative in Taiwan is KUO'S YUAN IN ENTERPRISE CO., LTD..

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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ec0633c12b44b5f06c0807848e9dbc0e
Registration Details
Taiwan FDA Registration: ec0633c12b44b5f06c0807848e9dbc0e
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Device Details

"Randox" Lithium 2
TW: "็‘žๅพทๅฃซ"้‹ฐ่ฉฆๅŠ‘
Risk Class 2
MD

Registration Details

ec0633c12b44b5f06c0807848e9dbc0e

Ministry of Health Medical Device Import No. 032419

DHA05603241905

Company Information

United Kingdom

Product Details

This product is used for in vitro diagnostic quantitative determination of lithium in serum. This product is suitable for RX series instruments including RX daytona and RX imola.

A Clinical chemistry and clinical toxicology

A3560 lithium test system

Imported from abroad

Dates and Status

May 03, 2019

May 03, 2024