Taiwan FDA registration 08f7b13ec3fdfb9fbfe3ccb5415787ea

"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 28, 2011 – Dec 28, 2016Cancelled
Registration details
Analysis ID
08f7b13ec3fdfb9fbfe3ccb5415787ea
Customs Code
DHA04401124202
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 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
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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 08f7b13ec3fdfb9fbfe3ccb5415787ea 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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