Taiwan FDA registration 1f93bf3ff4f281ccc333e8d51a351573
Prismaflex oXiris Set
TW: 百希瑞血液淨化治療套組
Taiwan·Risk Class 2·MD·GAMBRO INDUSTRIES·Registered Nov 26, 2018 – Nov 26, 2028ActiveRegistration details
- Analysis ID
- 1f93bf3ff4f281ccc333e8d51a351573
- License Form
- Ministry of Health Medical Device Import No. 031718
- Customs Code
- DHA05603171800
Company information
- Manufacturer
- GAMBRO INDUSTRIES
- Manufacturer Country
- France
- Authorized Representative
- BAXTER HEALTHCARE LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H5860 Highly permeable hemodialysis system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 26, 2018
- Expiry Date
- Nov 26, 2028
About this record
Access comprehensive regulatory information for Prismaflex oXiris Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1f93bf3ff4f281ccc333e8d51a351573 and manufactured by GAMBRO INDUSTRIES. The authorized representative in Taiwan is BAXTER HEALTHCARE LTD..
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