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Legicobacterium Legionella antibody reagent (unsterilized)  - Taiwan Registration eb04f76c86ef23b1f10760edcc065b30

Access comprehensive regulatory information for Legicobacterium Legionella antibody reagent (unsterilized)  in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number eb04f76c86ef23b1f10760edcc065b30 and manufactured by EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG. The authorized representative in Taiwan is SEEKERS BIOMEDICAL CO., LTD..

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eb04f76c86ef23b1f10760edcc065b30
Registration Details
Taiwan FDA Registration: eb04f76c86ef23b1f10760edcc065b30
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Device Details

Legicobacterium Legionella antibody reagent (unsterilized) 
TW: 協克退伍軍人桿菌抗體試劑(未滅菌) 
Risk Class 1

Registration Details

eb04f76c86ef23b1f10760edcc065b30

DHA04400923207

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 嗜血桿菌屬血清試劑

import

Dates and Status

Sep 23, 2010

Sep 23, 2025