"AMERITEK" Legionella-Ag test (Non-Sterile) - Taiwan Registration 0dc781c9dd9d4bb21d0b3049ae1d7ce3
Access comprehensive regulatory information for "AMERITEK" Legionella-Ag test (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0dc781c9dd9d4bb21d0b3049ae1d7ce3 and manufactured by AMERITEK, INC.. The authorized representative in Taiwan is APPLIED BIOTECH ENTERPRISE CO., LTD..
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Device Details
Registration Details
0dc781c9dd9d4bb21d0b3049ae1d7ce3
Ministry of Health Medical Device Import No. 013645
DHA09401364501
Product Details
Limit the management method of medical equipment Haemophilus serogenus (C.3300) first level identification range.
C Immunology and microbiology devices
C3300 Haemophilus serology
Imported from abroad
Dates and Status
Nov 29, 2013
Nov 29, 2023