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"Microgen" Staph Rapid Test (Non-Sterile) - Taiwan Registration 8b664742d6370bef0e820da4c97b261a

Access comprehensive regulatory information for "Microgen" Staph Rapid Test (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8b664742d6370bef0e820da4c97b261a and manufactured by MICROGEN BIOPRODUCTS LTD. The authorized representative in Taiwan is GLOWAY 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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8b664742d6370bef0e820da4c97b261a
Registration Details
Taiwan FDA Registration: 8b664742d6370bef0e820da4c97b261a
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Device Details

"Microgen" Staph Rapid Test (Non-Sterile)
TW: "้‚ๅ…‹ๅฅ‡"้‡‘้ปƒ่‰ฒ่‘ก่„็ƒ่Œไนณ่† ๅ‡้›†ๆธฌๅฎš่ฉฆๅŠ‘็ต„ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

8b664742d6370bef0e820da4c97b261a

Ministry of Health Medical Device Import No. 019305

DHA09401930507

Company Information

United Kingdom

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 devices

C3700 Staphylococcus aureus serum reagent

Imported from abroad

Dates and Status

Jul 13, 2018

Jul 13, 2023