"DiaSorin" Mycoplasma pneumoniae CLIA KIT (Non-Sterile)
Taiwan·Risk Class 1·MD·DIASORIN IRELAND LTD.·Registered Aug 10, 2015 – Aug 10, 2020Cancelled- Analysis ID
- 4321d873cfdff3b8bb528d579ddea0a1
- License Form
- Ministry of Health Medical Device Import No. 015567
- Customs Code
- DHA09401556704
- Manufacturer
- DIASORIN IRELAND LTD.
- Manufacturer Country
- Ireland
- Authorized Representative
- EVERLIGHT BIOTECH(TAIWAN) CO., LTD.
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3375 Mycoplasma serum reagent
- Import Information
- Imported from abroad
- Registration Date
- Aug 10, 2015
- Expiry Date
- Aug 10, 2020
- Cancellation Date
- May 19, 2022
- Status
- Logged out
- Reason
- 許可證逾有效期未申請展延
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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 4321d873cfdff3b8bb528d579ddea0a1 and manufactured by DIASORIN IRELAND LTD.. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) 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.