"Vircell" Legionella pneumophila Assay (Non-sterile) - Taiwan Registration 23c14bdc388730f7fa356fa8ca8cf29f
Access comprehensive regulatory information for "Vircell" Legionella pneumophila Assay (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 23c14bdc388730f7fa356fa8ca8cf29f and manufactured by VIRCELL, S.L. The authorized representative in Taiwan is Abbott Rapid Diagnostics Health Corp..
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
Registration Details
23c14bdc388730f7fa356fa8ca8cf29f
Ministry of Health Medical Device Import No. 019028
DHA09401902807
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
May 07, 2018
May 07, 2028

