Taiwan FDA registration 16e9d7b25744aab4cdc80914b428dc2e
“DiaSorin” Q Fever IFA IgG (Non-Sterile)
TW: “豐技”Q熱非直接免疫螢光抗體試驗--IgG(未滅菌)
Taiwan·Risk Class 1·MD·DiaSorin Molecular LLC·Registered May 06, 2019 – May 06, 2024ExpiredRegistration details
- Analysis ID
- 16e9d7b25744aab4cdc80914b428dc2e
- License Form
- Ministry of Health Medical Device Import No. 020400
- Customs Code
- DHA09402040001
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” Q Fever 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 16e9d7b25744aab4cdc80914b428dc2e and manufactured by DiaSorin Molecular LLC. The authorized representative in Taiwan is FENG CHI BIOTECH CORP..
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