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In vitro test for Corris Legionnaires bacteria (unsterilized) - Taiwan Registration 2a717107e0ba562e1e59394d5e266964

Access comprehensive regulatory information for In vitro test for Corris 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 2a717107e0ba562e1e59394d5e266964 and manufactured by CORIS BIOCONCEPT. 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.

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2a717107e0ba562e1e59394d5e266964
Registration Details
Taiwan FDA Registration: 2a717107e0ba562e1e59394d5e266964
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Device Details

In vitro test for Corris Legionnaires bacteria (unsterilized)
TW: ็ง‘้‡Œๆ–ฏ้€€ไผ่ปไบบ่Œ้ซ”ๅค–่ฉฆ้ฉ—(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

2a717107e0ba562e1e59394d5e266964

DHA04400925009

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

Sep 24, 2010

Sep 24, 2020

May 19, 2022

Cancellation Information

Logged out

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