Taiwan FDA registration 931ce38adc4fd03454a67d1b29889da2
“ALIFAX” Automated sedimentation rate device (Non-sterile)
TW: "希森美康"全自動紅血球沉降速率儀(未滅菌)
Taiwan·Risk Class 1·MD·Alifax S.r.l.·Registered Jun 12, 2014 – Jun 12, 2024ExpiredRegistration details
- Analysis ID
- 931ce38adc4fd03454a67d1b29889da2
- License Form
- Ministry of Health Medical Device Import No. 014238
- Customs Code
- DHA09401423806
Company information
- Manufacturer
- Alifax S.r.l.
- Manufacturer Country
- Italy
- Authorized Representative
- SYSMEX TAIWAN CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Automatic Sedimentation Rate Device (B.5800)".
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B5800 Automatic Settling Rate Device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 12, 2014
- Expiry Date
- Jun 12, 2024
About this record
Access comprehensive regulatory information for “ALIFAX” Automated sedimentation rate device (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 931ce38adc4fd03454a67d1b29889da2 and manufactured by Alifax S.r.l.. The authorized representative in Taiwan is SYSMEX TAIWAN CO., LTD..
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