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"Quick test" Listeria rapid test reagent (unsterilized) - Taiwan Registration 1f478815b58ce0d042d20398e7d11b5e

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..

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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1f478815b58ce0d042d20398e7d11b5e
Registration Details
Taiwan FDA Registration: 1f478815b58ce0d042d20398e7d11b5e
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Device Details

"Quick test" Listeria rapid test reagent (unsterilized)
TW: โ€œ้€Ÿๆธฌโ€ๆŽๆ–ฏ็‰น่Œๅฟซ้€Ÿๆชข้ฉ—่ฉฆๅŠ‘(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

1f478815b58ce0d042d20398e7d11b5e

DHA04401156704

Company Information

Spain

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Listeria sera reagent (C.3355)".

C Immunology and microbiology

C.3355 ๆŽๆ–ฏ็‰นๆฐ่Œๅฑฌ่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Apr 06, 2012

Apr 06, 2017

Jan 10, 2019

Cancellation Information

Logged out

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