Taiwan FDA registration c45fe725058d5fca7e24737f01bbc91e
“Diasorin” Chlamydia MIF IgG Kit (Non sterile)
TW: “豐技”披衣菌微免疫螢光IgG試驗套組 (未滅菌)
Taiwan·Risk Class 1·MD·DiaSorin Molecular LLC·Registered Apr 25, 2019 – Apr 25, 2024ExpiredRegistration details
- Analysis ID
- c45fe725058d5fca7e24737f01bbc91e
- License Form
- Ministry of Health Medical Device Import No. 020368
- Customs Code
- DHA09402036805
Company information
- Manufacturer
- DiaSorin Molecular LLC
- Manufacturer Country
- United States
- Authorized Representative
- FENG CHI BIOTECH CORP.
Product details
- Intended Use
- Limited to the first level identification range of Chlamydomydia serum reagent (C.3120) of medical device management methods.
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3120 Chlamydia serum reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 25, 2019
- Expiry Date
- Apr 25, 2024
About this record
Access comprehensive regulatory information for “Diasorin” Chlamydia MIF IgG 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 c45fe725058d5fca7e24737f01bbc91e and manufactured by DiaSorin Molecular LLC. The authorized representative in Taiwan is FENG CHI BIOTECH CORP..
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