Taiwan FDA registration acf3f196b38ebb9c9c35e322be6426c2
SD BIOSENSOR STANDARD F Legionella Ag FIA (Non-Sterile)
TW: “速得百森”退伍軍人症螢光酵素免疫分析檢測套組(未滅菌)
Taiwan·Risk Class 1·MD·SD BIOSENSOR,INC.·Registered Jan 16, 2019 – Jan 16, 2024ExpiredRegistration details
- Analysis ID
- acf3f196b38ebb9c9c35e322be6426c2
- License Form
- Ministry of Health Medical Device Import No. 020030
- Customs Code
- DHA09402003007
Company information
- Manufacturer
- SD BIOSENSOR,INC.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- CREATIVE LIFE SCIENCE CO., LTD.
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
- Jan 16, 2019
- Expiry Date
- Jan 16, 2024
About this record
Access comprehensive regulatory information for SD BIOSENSOR STANDARD F Legionella Ag FIA (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 acf3f196b38ebb9c9c35e322be6426c2 and manufactured by SD BIOSENSOR,INC.. The authorized representative in Taiwan is CREATIVE LIFE SCIENCE CO., LTD..
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