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“Boditech” AFIAS-6 Analyzer (Non-Sterile) - Taiwan Registration 585308d9078df29f1a2f00e39384f4b1

Access comprehensive regulatory information for “Boditech” AFIAS-6 Analyzer (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 585308d9078df29f1a2f00e39384f4b1 and manufactured by Boditech Med Inc.. The authorized representative in Taiwan is PROGRESSIVE GROUP INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Boditech Med Inc., and 1 recent registrations in the same category. 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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585308d9078df29f1a2f00e39384f4b1
Registration Details
Taiwan FDA Registration: 585308d9078df29f1a2f00e39384f4b1
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Device Details

“Boditech” AFIAS-6 Analyzer (Non-Sterile)
TW: “巴迪泰” 自動化螢光免疫分析系統(未滅菌)
Risk Class 1
MD

Registration Details

585308d9078df29f1a2f00e39384f4b1

Ministry of Health Medical Device Import Registration No. 022470

DHA08402247000

Company Information

Korea, Republic of

Product Details

Limited to the first level identification range of the "Individual Photometric Chemical Analyzer for Clinical Use (A.2160)" of the Measures for the Administration of Medical Devices.

A Clinical chemistry and clinical toxicology

A2160 Individual photometric chemistry analyzer for clinical use

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2026

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