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Treponema pallidum hemoagglutination reagent - Taiwan Registration be418389a9f27e67daff14919c6cdac2

Access comprehensive regulatory information for Treponema pallidum hemoagglutination reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number be418389a9f27e67daff14919c6cdac2 and manufactured by OMEGA DIAGNOSTICS LTD.. The authorized representative in Taiwan is EUGENE-CHEN 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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be418389a9f27e67daff14919c6cdac2
Registration Details
Taiwan FDA Registration: be418389a9f27e67daff14919c6cdac2
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Device Details

Treponema pallidum hemoagglutination reagent
TW: ๅฅง็ฑณๅŠ ๆข…ๆฏ’่žบๆ—‹้ซ”่ก€็ƒๅ‡้›†่ฉฆๅŠ‘
Risk Class 2
Cancelled

Registration Details

be418389a9f27e67daff14919c6cdac2

DHA00601615907

Company Information

United Kingdom

Product Details

่ขซๅ‹•่ก€็ƒๅ‡้›†ๆณ•ๆธฌ่ฉฆไบบ้ซ”่ก€ๆธ…ๆˆ–่…ฆ่„Š้ซ“ๆถฒไธญ็š„ๆข…ๆฏ’่žบๆ—‹้ซ”(Treponema pallidum)ๆŠ—้ซ”.

C Immunology and microbiology

C.3830 Treponema pallidum test

import

Dates and Status

Mar 15, 2006

Mar 15, 2021

Jun 22, 2022

Cancellation Information

Logged out

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