Taiwan FDA registration 582f720e506172f155434d655b49bda4
“Diasorin” Chlamydia MIF IgM Kit (Non sterile)
TW: “豐技”披衣菌微免疫螢光IgM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
- 582f720e506172f155434d655b49bda4
- License Form
- Ministry of Health Medical Device Import No. 020369
- Customs Code
- DHA09402036907
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 IgM 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 582f720e506172f155434d655b49bda4 and manufactured by DiaSorin Molecular LLC. The authorized representative in Taiwan is FENG CHI BIOTECH CORP..
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