Taiwan FDA registration fe8d01e5975e62ef344b165ba086bf16
"bioMerieux" VITEK MS Mycobacterium/Nocardia Kit (Non-Sterile)
TW: "生物梅里埃" 分枝桿菌/奴卡氏菌前處理試劑組 (未滅菌)
Taiwan·Risk Class 1·MD·BIOMERIEUX SA·Registered Mar 16, 2017 – Mar 16, 2027ActiveRegistration details
- Analysis ID
- fe8d01e5975e62ef344b165ba086bf16
- License Form
- Ministry of Health Medical Device Import No. 017610
- Customs Code
- DHA09401761002
Company information
- Manufacturer
- BIOMERIEUX SA
- Manufacturer Country
- France
- Authorized Representative
- Hong Kong Commercial Mérieux S.p.A. Taiwan Branch
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Microbial Identification and Measurement Equipment (C.2660)".
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C2660 Microbial identification and assay equipment
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 16, 2017
- Expiry Date
- Mar 16, 2027
About this record
Access comprehensive regulatory information for "bioMerieux" VITEK MS Mycobacterium/Nocardia 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 fe8d01e5975e62ef344b165ba086bf16 and manufactured by BIOMERIEUX SA. The authorized representative in Taiwan is Hong Kong Commercial Mérieux S.p.A. Taiwan Branch.
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