Taiwan FDA registration 9f01d843839fc45532df621490c01b46

In vitro test for Legionnaires' bacteria (unsterilized)

TW: "寇芮斯" 退伍軍人菌體外試驗 (未滅菌)

Taiwan·Risk Class 1·CORIS BIOCONCEPT·Registered Apr 18, 2011 – Apr 18, 2016Cancelled

Registration details

Analysis ID: 9f01d843839fc45532df621490c01b46
Customs Code: DHA04401021507

Company information

Manufacturer: CORIS BIOCONCEPT
Manufacturer Country: Belgium
Authorized Representative: GHOPE INTERNATIONAL BIOTECHNOLOGY CO., LTD.

Product details

Intended Use: Limit the management method of medical equipment Haemophilus serogenus (C.3300) first level identification range.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.3300 嗜血桿菌屬血清試劑
Import Information: import

Dates and status

Registration Date: Apr 18, 2011
Expiry Date: Apr 18, 2016
Cancellation Date: Apr 25, 2018

Cancellation information

Status: Logged out
Reason: 自行鍵入

About this record

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..

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