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Xiecke trachoma antibody kit (unsterilized) - Taiwan Registration f2e1ec79576023d640af2652d3797abf

Access comprehensive regulatory information for Xiecke trachoma antibody kit (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f2e1ec79576023d640af2652d3797abf and manufactured by SAVYON DIAGNOSTICS LTD.. The authorized representative in Taiwan is SEEKERS BIOMEDICAL 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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f2e1ec79576023d640af2652d3797abf
Registration Details
Taiwan FDA Registration: f2e1ec79576023d640af2652d3797abf
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Device Details

Xiecke trachoma antibody kit (unsterilized)
TW: ๅ”ๅ…‹็ ‚็œผๅž‹ๆŠซ่กฃ่ŒๆŠ—้ซ”่ฉฆๅŠ‘ๅฅ—็ต„(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

f2e1ec79576023d640af2652d3797abf

DHA04400857700

Company Information

Israel

Product Details

It is limited to the first-level identification scope of Chlamydia serum reagent (C.3120) in the classification and grading management measures for medical devices.

C Immunology and microbiology

C.3120 ๆŠซ่กฃ่Œ่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Mar 01, 2010

Mar 01, 2030