Taiwan FDA registration e1798f4c08150c2780b9094d1015ef04
“DiaSorin”Rickettsia IFA IgG(non-sterile)
TW: “豐技”立克次體IgG玻片檢測套組(未滅菌)
Taiwan·Risk Class 1·MD·DiaSorin Molecular LLC·Registered May 06, 2019 – May 06, 2024ExpiredRegistration details
- Analysis ID
- e1798f4c08150c2780b9094d1015ef04
- License Form
- Ministry of Health Medical Device Import No. 020404
- Customs Code
- DHA09402040409
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 Rickettsial serum reagent (C.3500) of the management method for medical devices.
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3500 rickettsial serum reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 06, 2019
- Expiry Date
- May 06, 2024
About this record
Access comprehensive regulatory information for “DiaSorin”Rickettsia IFA IgG(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 e1798f4c08150c2780b9094d1015ef04 and manufactured by DiaSorin Molecular LLC. The authorized representative in Taiwan is FENG CHI BIOTECH CORP..
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