Taiwan FDA registration 1f478815b58ce0d042d20398e7d11b5e

"Quick test" Listeria rapid test reagent (unsterilized)

TW: “速測”李斯特菌快速檢驗試劑(未滅菌)

Taiwan·Risk Class 1·CERTEST BIOTEC S.L.·Registered Apr 06, 2012 – Apr 06, 2017Cancelled

Registration details

Analysis ID: 1f478815b58ce0d042d20398e7d11b5e
Customs Code: DHA04401156704

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 "Listeria sera reagent (C.3355)".
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.3355 李斯特氏菌屬血清試劑
Import Information: import

Dates and status

Registration Date: Apr 06, 2012
Expiry Date: Apr 06, 2017
Cancellation Date: Jan 10, 2019

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期;;自請註銷

About this record

Access comprehensive regulatory information for "Quick test" Listeria 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 1f478815b58ce0d042d20398e7d11b5e and manufactured by CERTEST BIOTEC S.L.. The authorized representative in Taiwan is JOLEX INTERNATIONAL CO., LTD..

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