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Staphylococcus Poliber Rapid Latex Agglutination Kit (Unsterilized) - Taiwan Registration 397b0d5536e74f9ac2fd1871c06e705c

Access comprehensive regulatory information for Staphylococcus Poliber Rapid Latex Agglutination 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 397b0d5536e74f9ac2fd1871c06e705c and manufactured by PRO-LAB, INC.. The authorized representative in Taiwan is METEK LAB INC..

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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397b0d5536e74f9ac2fd1871c06e705c
Registration Details
Taiwan FDA Registration: 397b0d5536e74f9ac2fd1871c06e705c
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Device Details

Staphylococcus Poliber Rapid Latex Agglutination Kit (Unsterilized)
TW: ๆณขๅŠ›ไผฏ่‘ก่„็ƒ่Œๅฟซ้€Ÿไนณ่† ๅ‡้›†่ฉฆๅŠ‘็ต„ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

397b0d5536e74f9ac2fd1871c06e705c

DHA04400523802

Company Information

Canada

Product Details

It is limited to the first-level identification scope of the "Staphylococcus aureus serum reagent (C.3700)" of the classification and grading management measures for medical devices.

C Immunology and microbiology

C.3700 ้‡‘้ปƒ่‰ฒ่‘ก่„็ƒ่Œ่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Oct 17, 2006

Oct 17, 2026