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"Badiec" Efia immunofluorescence analyzer (unsterilized) - Taiwan Registration 748ef173b061c72464706d945e522daf

Access comprehensive regulatory information for "Badiec" Efia 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 748ef173b061c72464706d945e522daf 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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748ef173b061c72464706d945e522daf
Registration Details
Taiwan FDA Registration: 748ef173b061c72464706d945e522daf
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Device Details

"Badiec" Efia immunofluorescence analyzer (unsterilized)
TW: "ๅทด่ฟช้ตๅ…‹" ่‰พ่ฒ้›…ไป•ๅ…็–ซ่žขๅ…‰ๅˆ†ๆžๅ„€ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

748ef173b061c72464706d945e522daf

DHA084a0021709

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

Aug 29, 2023

Oct 31, 2025