Taiwan FDA registration 4ad90f5d3a8b165ff2135b5378b3b7c4

"Quick test" pylori rapid test reagent (unsterilized)

TW: "速測"幽門桿菌快速檢驗試劑(未滅菌)

Taiwan·Risk Class 1·CERTEST BIOTEC S.L.·Registered Dec 28, 2011 – Dec 28, 2016Cancelled

Registration details

Analysis ID: 4ad90f5d3a8b165ff2135b5378b3b7c4
Customs Code: DHA04401124100

Company information

Manufacturer: CERTEST BIOTEC S.L.
Manufacturer Country: Spain
Authorized Representative: JOLEX INTERNATIONAL CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Helicobacter Serological Reagent (C.0003)".
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.0003 螺旋桿菌屬血清試劑
Import Information: import

Dates and status

Registration Date: Dec 28, 2011
Expiry Date: Dec 28, 2016
Cancellation Date: Mar 09, 2017

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Quick test" pylori rapid test reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4ad90f5d3a8b165ff2135b5378b3b7c4 and manufactured by CERTEST BIOTEC S.L.. The authorized representative in Taiwan is JOLEX INTERNATIONAL CO., LTD..

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