Taiwan FDA registration 4aadb4b436d1df300bf7e337fd501252

"Quick Test" Rotavirus Rapid Test Reagent (Unsterilized)

TW: "速測" 輪狀病毒快速檢驗試劑 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·CERTEST BIOTEC, S.L.·Registered Dec 14, 2016 – Dec 14, 2021Cancelled
Registration details
Analysis ID
4aadb4b436d1df300bf7e337fd501252
Customs Code
DHA09401728201
Company information
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 "Polio Virus Serological Reagent (C.3405)".
Product Type (Level 1)
C Immunology and microbiology
Product Type (Level 2)
C.3405 Poliomyelitis virus serum reagent
Import Information
import
Dates and status
Registration Date
Dec 14, 2016
Expiry Date
Dec 14, 2021
Cancellation Date
Mar 07, 2022
Cancellation information
Status
Logged out
Reason
屆期未申請展延;;自請註銷
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About this record

Access comprehensive regulatory information for "Quick Test" Rotavirus 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 4aadb4b436d1df300bf7e337fd501252 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, 1 companies making similar products including CERTEST BIOTEC S.L., and 1 recent registrations in the same category. 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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