Taiwan FDA registration 55857c6021825360ffc4b0aa7fd99e98

"CerTest" Streptococcus Pneumoniae (Non-Sterile)

TW: "攝特司" 肺炎鏈球菌尿液抗原快速診斷試劑 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·CERTEST BIOTEC S.L.·Registered Oct 29, 2020 – Oct 29, 2025Expired
Registration details
Analysis ID
55857c6021825360ffc4b0aa7fd99e98
License Form
Ministry of Health Medical Device Import No. 022069
Customs Code
DHA09402206905
Company information
Manufacturer Country
Spain
Authorized Representative
MEDTRI CO., LTD.
Product details
Intended Use
Restriction of medical device management methods Streptococcus belongs to the first level identification range of serum reagent (C.3740).
Product Type (Level 1)
C Immunology and microbiology devices
Product Type (Level 2)
C3740 Streptococcus serology
Import Information
Imported from abroad
Dates and status
Registration Date
Oct 29, 2020
Expiry Date
Oct 29, 2025
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About this record

Access comprehensive regulatory information for "CerTest" Streptococcus Pneumoniae (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 55857c6021825360ffc4b0aa7fd99e98 and manufactured by CERTEST BIOTEC S.L.. The authorized representative in Taiwan is MEDTRI 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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