"DiaSorin" Mycoplasma pneumoniae CLIA KIT (Non-Sterile)
Taiwan·Risk Class 1·MD·DIASORIN IRELAND LTD.·Registered Jan 09, 2017 – Jan 09, 2022Expired- Analysis ID
- ae14fac482c66620d09a8168f14282af
- License Form
- Ministry of Health Medical Device Import No. 017383
- Customs Code
- DHA09401738304
- Manufacturer
- DIASORIN IRELAND LTD.
- Manufacturer Country
- Ireland
- Authorized Representative
- MEDRICH INSTRUMENT CO., LTD.
- 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
- Registration Date
- Jan 09, 2017
- Expiry Date
- Jan 09, 2022
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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 ae14fac482c66620d09a8168f14282af and manufactured by DIASORIN IRELAND LTD.. The authorized representative in Taiwan is MEDRICH INSTRUMENT CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including DIASORIN ITALIA S.P.A., 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.