Taiwan FDA registration 6bd672f6384eb3a58bb364f63ab83c92

"DiaSorin" Mycoplasma pneumoniae CLIA KIT (Non-Sterile)

TW: "戴思林" 黴漿菌肺炎化學冷光檢驗試劑組 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·DIASORIN ITALIA S.P.A.·Registered Jan 25, 2019 – Jan 25, 2024Expired
Registration details
Analysis ID
6bd672f6384eb3a58bb364f63ab83c92
License Form
Ministry of Health Medical Device Import No. 020061
Customs Code
DHA09402006105
Company information
Manufacturer Country
Italy
Authorized Representative
EVERLIGHT BIOTECH(TAIWAN) CO., LTD.
Product details
Intended Use
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Mycoplasma Serological Reagent (C.3375)".
Product Type (Level 1)
C Immunology and microbiology devices
Product Type (Level 2)
C3375 Mycoplasma serum reagent
Import Information
Imported from abroad
Dates and status
Registration Date
Jan 25, 2019
Expiry Date
Jan 25, 2024
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About this record

Access comprehensive regulatory information for "DiaSorin" Mycoplasma pneumoniae CLIA KIT (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 6bd672f6384eb3a58bb364f63ab83c92 and manufactured by DIASORIN ITALIA S.P.A.. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DIASORIN IRELAND LTD., and 2 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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