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Nofafer Human Mumps Virus Immunoglobulin G Enzyme Immunoassay Kit (Unsterilized) - Taiwan Registration e66e806c2e714c8d68c8512bbeae0c2e

Access comprehensive regulatory information for Nofafer Human Mumps Virus Immunoglobulin G Enzyme Immunoassay 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 e66e806c2e714c8d68c8512bbeae0c2e 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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e66e806c2e714c8d68c8512bbeae0c2e
Registration Details
Taiwan FDA Registration: e66e806c2e714c8d68c8512bbeae0c2e
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Device Details

Nofafer Human Mumps Virus Immunoglobulin G Enzyme Immunoassay Kit (Unsterilized)
TW: ่ซพๆณ•้ตไบบ้กžๆŠ—่…ฎ่…บ็‚Ž็—…ๆฏ’ๅ…็–ซ็ƒ่›‹็™ฝG้…ต็ด ๅ…็–ซๅˆ†ๆžๅฅ—็ต„(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

e66e806c2e714c8d68c8512bbeae0c2e

DHA04400297900

Company Information

Product Details

Qualitative detection of anti-mumps virus immunoglobulin G antibodies in human serum.

C Immunology and microbiology

C.3380 ่…ฎ่…บ็‚Ž็—…ๆฏ’่ก€ๆธ…่ฉฆๅŠ‘

Input;; QMS/QSD

Dates and Status

Mar 16, 2006

Mar 16, 2026