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In vitro test for Legionnaires' bacteria (unsterilized) - Taiwan Registration 9f01d843839fc45532df621490c01b46

Access comprehensive regulatory information for In vitro test for Legionnaires' bacteria (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9f01d843839fc45532df621490c01b46 and manufactured by CORIS BIOCONCEPT. The authorized representative in Taiwan is GHOPE INTERNATIONAL BIOTECHNOLOGY CO., LTD..

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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9f01d843839fc45532df621490c01b46
Registration Details
Taiwan FDA Registration: 9f01d843839fc45532df621490c01b46
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Device Details

In vitro test for Legionnaires' bacteria (unsterilized)
TW: "ๅฏ‡่Šฎๆ–ฏ" ้€€ไผ่ปไบบ่Œ้ซ”ๅค–่ฉฆ้ฉ— (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

9f01d843839fc45532df621490c01b46

DHA04401021507

Company Information

Belgium

Product Details

Limit the management method of medical equipment Haemophilus serogenus (C.3300) first level identification range.

C Immunology and microbiology

C.3300 ๅ—œ่ก€ๆกฟ่Œๅฑฌ่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Apr 18, 2011

Apr 18, 2016

Apr 25, 2018

Cancellation Information

Logged out

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