Taiwan FDA registration dbfc869745fa63e189b7fa277550d6ed
"Novatec" NovaLisa Coxiella burnetii (Q-Fever) Phase 1 IgG (Non-Sterile)
TW: "諾瓦德" 諾瓦莉莎Q熱第一階段IgG酵素免疫試驗組 (未滅菌)
Taiwan·Risk Class 1·MD·NOVATEC IMMUNDIAGNOSTICA GMBH·Registered Jan 11, 2016 – Jan 11, 2021ExpiredRegistration details
- Analysis ID
- dbfc869745fa63e189b7fa277550d6ed
- License Form
- Ministry of Health Medical Device Import No. 016066
- Customs Code
- DHA09401606600
Company information
- Manufacturer
- NOVATEC IMMUNDIAGNOSTICA GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- STANDARD MOLECULES INC.
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
- Jan 11, 2016
- Expiry Date
- Jan 11, 2021
About this record
Access comprehensive regulatory information for "Novatec" NovaLisa Coxiella burnetii (Q-Fever) Phase 1 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 dbfc869745fa63e189b7fa277550d6ed and manufactured by NOVATEC IMMUNDIAGNOSTICA GMBH. The authorized representative in Taiwan is STANDARD MOLECULES INC..
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