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"Ruicheng" Bairka Chlamydomydomia pneumoniae IgM screening reagent (unsterilized) - Taiwan Registration f7b8d497cd1d7cb821316a7131a37d47

Access comprehensive regulatory information for "Ruicheng" Bairka Chlamydomydomia pneumoniae IgM screening reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f7b8d497cd1d7cb821316a7131a37d47 and manufactured by Labsystems Diagnostics Oy. The authorized representative in Taiwan is RAFA INTERNATIONAL CORP..

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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f7b8d497cd1d7cb821316a7131a37d47
Registration Details
Taiwan FDA Registration: f7b8d497cd1d7cb821316a7131a37d47
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Device Details

"Ruicheng" Bairka Chlamydomydomia pneumoniae IgM screening reagent (unsterilized)
TW: "้Šณ่ช " ๆ‹œ็ˆพๅก่‚บ็‚ŽๆŠซ่กฃ่ŒIgM็ฏฉๆชข่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

f7b8d497cd1d7cb821316a7131a37d47

DHA04401268808

Company Information

Finland

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

Feb 07, 2013

Feb 07, 2028