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"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.

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23c14bdc388730f7fa356fa8ca8cf29f
Registration Details
Taiwan FDA Registration: 23c14bdc388730f7fa356fa8ca8cf29f
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Device Details

"Vircell" Legionella pneumophila Assay (Non-sterile)
TW: "ๅ‡ก่ณฝ็ˆพ" ้€€ไผ่ปไบบๆกฟ่Œๆชขๆธฌๅฅ—็ต„(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

23c14bdc388730f7fa356fa8ca8cf29f

Ministry of Health Medical Device Import No. 019028

DHA09401902807

Company Information

Spain

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