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Boli Staphylococcus aureus rapid latex agglutination test group (unsterilized) - Taiwan Registration 4a8913a8ae5ad81c73834d537bf0d172

Access comprehensive regulatory information for Boli Staphylococcus aureus rapid latex agglutination test group (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4a8913a8ae5ad81c73834d537bf0d172 and manufactured by PRO-LAB, INC.. The authorized representative in Taiwan is SANCORDON 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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4a8913a8ae5ad81c73834d537bf0d172
Registration Details
Taiwan FDA Registration: 4a8913a8ae5ad81c73834d537bf0d172
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Device Details

Boli Staphylococcus aureus rapid latex agglutination test group (unsterilized)
TW: ๆณขๅŠ›ๅšๆณขๅŠ›้‡‘้ปƒ่‰ฒ่‘ก่„็ƒ่Œๅฟซ้€Ÿไนณ่† ๅ‡้›†่ฉฆ้ฉ—็ต„(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

4a8913a8ae5ad81c73834d537bf0d172

DHA04400799306

Company Information

Canada

Product Details

Limited to the first level identification range of the "Staphylococcus aureus serum reagent (C.3700)" of the Measures for the Administration of Medical Devices.

C Immunology and microbiology

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

import

Dates and Status

Aug 25, 2009

Aug 25, 2019

Aug 05, 2022

Cancellation Information

Logged out

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