Taiwan FDA registration fbba6bdf466d05ddeeeb4dbcff751321
"CerTest" Legionella (Non-Sterile)
TW: "攝特司" 退伍軍人肺炎尿液抗原快速診斷試劑 (未滅菌)
Taiwan·Risk Class 1·MD·CERTEST BIOTEC S.L.·Registered Oct 29, 2020 – Oct 29, 2025ExpiredRegistration details
- Analysis ID
- fbba6bdf466d05ddeeeb4dbcff751321
- License Form
- Ministry of Health Medical Device Import No. 022068
- Customs Code
- DHA09402206803
Company information
- Manufacturer
- CERTEST BIOTEC S.L.
- Manufacturer Country
- Spain
- Authorized Representative
- MEDTRI 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
- Oct 29, 2020
- Expiry Date
- Oct 29, 2025
About this record
Access comprehensive regulatory information for "CerTest" Legionella (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 fbba6bdf466d05ddeeeb4dbcff751321 and manufactured by CERTEST BIOTEC S.L.. The authorized representative in Taiwan is MEDTRI CO., LTD..
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