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"Barditek" Ekoma Immunofluorescence Analyzer (Unsterilized) - Taiwan Registration 8d94717f9dae15305e256cb8b2f5cd4d

Access comprehensive regulatory information for "Barditek" Ekoma Immunofluorescence Analyzer (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8d94717f9dae15305e256cb8b2f5cd4d and manufactured by Boditech Med Inc.. The authorized representative in Taiwan is MEDRICH INSTRUMENT 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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8d94717f9dae15305e256cb8b2f5cd4d
Registration Details
Taiwan FDA Registration: 8d94717f9dae15305e256cb8b2f5cd4d
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Device Details

"Barditek" Ekoma Immunofluorescence Analyzer (Unsterilized)
TW: "ๅทด่ฟช้ตๅ…‹" ่‰พ้—Š็‘ชๅ…็–ซ่žขๅ…‰ๅˆ†ๆžๅ„€ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

8d94717f9dae15305e256cb8b2f5cd4d

DHA084a0018101

Company Information

Korea, Republic of

Product Details

Limited to the classification and grading management measures of medical equipment "fluorescence instrument for clinical use (A.2560)" the first level identification range.

A Clinical chemistry and clinical toxicology

A.2560 Fluorometer for clinical use

Dates and Status

May 24, 2023

Oct 31, 2025