Legionella latex agglutination kit (unsterilized) - Taiwan Registration 4ab0e082b5218d2f757e420a1c607cbb
Access comprehensive regulatory information for Legionella latex agglutination 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 4ab0e082b5218d2f757e420a1c607cbb and manufactured by LIOFILCHEM S.R.L.. The authorized representative in Taiwan is DYBO ENTERPRISE COMPANY LIMITED.
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.
Device Details
Product Details
Limit the management method of medical equipment Haemophilus serogenus (C.3300) first level identification range.
C Immunology and microbiology
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import
Dates and Status
Aug 30, 2011
Aug 30, 2016
May 28, 2018
Cancellation Information
Logged out
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