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"Ruicheng" Bairka pneumoniae IgM screening reagent (unsterilized) - Taiwan Registration 7c4b0a904d8ae8937550c1bd85b28841

Access comprehensive regulatory information for "Ruicheng" Bairka 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 7c4b0a904d8ae8937550c1bd85b28841 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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7c4b0a904d8ae8937550c1bd85b28841
Registration Details
Taiwan FDA Registration: 7c4b0a904d8ae8937550c1bd85b28841
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Device Details

"Ruicheng" Bairka pneumoniae IgM screening reagent (unsterilized)
TW: โ€œ้Šณ่ช โ€ๆ‹œ็ˆพๅก่‚บ็‚Ž้ปดๆผฟ่ŒIgM็ฏฉๆชข่ฉฆๅŠ‘(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

7c4b0a904d8ae8937550c1bd85b28841

DHA04401177307

Company Information

Finland

Product Details

Limited to the classification and grading management method of medical equipment, the first level identification range of "Mycoplasma serum reagent (C.3375)".

C Immunology and microbiology

C.3375 ้ปดๆผฟ่Œๅฑฌ่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

May 31, 2012

May 31, 2027