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Nofafer Human Antivaricella Zoster Virus Immunoglobulin M Enzyme Immunoassay Set - Taiwan Registration dcc7140e2ab1b6e9272981f6f305734e

Access comprehensive regulatory information for Nofafer Human Antivaricella Zoster Virus Immunoglobulin M Enzyme Immunoassay Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dcc7140e2ab1b6e9272981f6f305734e and manufactured by GOLD STANDARD DIAGNOSTICS FRANKFURT GMBH. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) CO., LTD..

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dcc7140e2ab1b6e9272981f6f305734e
Registration Details
Taiwan FDA Registration: dcc7140e2ab1b6e9272981f6f305734e
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Device Details

Nofafer Human Antivaricella Zoster Virus Immunoglobulin M Enzyme Immunoassay Set
TW: ่ซพๆณ•้ตไบบ้กžๆŠ—ๆฐด็—˜ๅธถ็‹€็šฐ็–น็—…ๆฏ’ๅ…็–ซ็ƒ่›‹็™ฝM้…ต็ด ๅ…็–ซๅˆ†ๆžๅฅ—็ต„
Risk Class 2

Registration Details

dcc7140e2ab1b6e9272981f6f305734e

DHA00601727603

Company Information

Product Details

Enzyme immunoassay was used to legally detect immunoglobulin M classified antibodies against human varicella zoster virus in human serum.

C Immunology and microbiology

C.3900 Varicella Disease Poison Serum Trial

import

Dates and Status

Aug 11, 2006

Aug 11, 2026