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"Nofaferri" Legionnaires' Disease Test Set (Unsterilized) - Taiwan Registration 504f1ff904d9c0bacca6482e3936c6af

Access comprehensive regulatory information for "Nofaferri" Legionnaires' Disease Test Set (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 504f1ff904d9c0bacca6482e3936c6af and manufactured by GOLD STANDARD DIAGNOSTICS FRANKFURT GMBH. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) 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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504f1ff904d9c0bacca6482e3936c6af
Registration Details
Taiwan FDA Registration: 504f1ff904d9c0bacca6482e3936c6af
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Device Details

"Nofaferri" Legionnaires' Disease Test Set (Unsterilized)
TW: "่ซพๆณ•้ต" ้€€ไผ่ปไบบ็—‡ๆชข้ฉ—่ฉฆๅŠ‘็ต„ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

504f1ff904d9c0bacca6482e3936c6af

DHA09401851500

Company Information

Product Details

It is limited to the first-level identification scope of Haemophilus serum reagent (C.3300) in the classification and grading management method of medical devices.

C Immunology and microbiology

C.3300 ๅ—œ่ก€ๆกฟ่Œๅฑฌ่ก€ๆธ…่ฉฆๅŠ‘

Input;; QMS/QSD

Dates and Status

Nov 16, 2017

Nov 16, 2027