Taiwan FDA registration bd00a5223ea479b4e90e881a6542d043
"Novatec" NovaLisa Legionella pneumophila IgM ELISA (Non-Sterile)
TW: "諾瓦德" 諾瓦莉莎嗜肺軍團病桿菌IgM酵素免疫試驗組 (未滅菌)
Taiwan·Risk Class 1·MD·NOVATEC IMMUNDIAGNOSTICA GMBH·Registered Mar 21, 2016 – Mar 21, 2021ExpiredRegistration details
- Analysis ID
- bd00a5223ea479b4e90e881a6542d043
- License Form
- Ministry of Health Medical Device Import No. 016280
- Customs Code
- DHA09401628002
Company information
- Manufacturer
- NOVATEC IMMUNDIAGNOSTICA GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- STANDARD MOLECULES INC.
Product details
- Intended Use
- Limit the management method of medical equipment Haemophilus serogenus (C.3300) first level identification range.
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3300 Haemophilus serology
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 21, 2016
- Expiry Date
- Mar 21, 2021
About this record
Access comprehensive regulatory information for "Novatec" NovaLisa Legionella pneumophila IgM ELISA (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 bd00a5223ea479b4e90e881a6542d043 and manufactured by NOVATEC IMMUNDIAGNOSTICA GMBH. The authorized representative in Taiwan is STANDARD MOLECULES INC..
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