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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Device Details
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

