Taiwan FDA registration 5706287c742f27f9f3848c49db64bfb6

"Quick Test" E. coli Rapid Test Reagent (Unsterilized)

TW: "速測" 大腸桿菌快速檢驗試劑 (未滅菌)

Taiwan·Risk Class 1·CERTEST BIOTEC S.L.·Registered Dec 29, 2011 – Dec 29, 2016Cancelled

Registration details

Analysis ID: 5706287c742f27f9f3848c49db64bfb6
Customs Code: DHA04401124508

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 "E. coli Serological Reagent (C.3255)".
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.3255 Escherichia coli serum test
Import Information: import

Dates and status

Registration Date: Dec 29, 2011
Expiry Date: Dec 29, 2016
Cancellation Date: Mar 14, 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" E. coli 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 5706287c742f27f9f3848c49db64bfb6 and manufactured by CERTEST BIOTEC S.L.. The authorized representative in Taiwan is JOLEX INTERNATIONAL CO., LTD..

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