Taiwan FDA registration e296c5be0d1fd8738783d7618f7f7293
“Baxter” Theranova
TW: “百特”特腎力血液透析器
Taiwan·Risk Class 2·MD·GAMBRO DIALYSATOREN GMBH·Registered Jan 16, 2018 – Jan 16, 2028ActiveRegistration details
- Analysis ID
- e296c5be0d1fd8738783d7618f7f7293
- License Form
- Ministry of Health Medical Device Import No. 030686
- Customs Code
- DHA05603068605
Company information
- Manufacturer
- GAMBRO DIALYSATOREN GMBH
- Manufacturer Country
- Germany
- 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
- Jan 16, 2018
- Expiry Date
- Jan 16, 2028
About this record
Access comprehensive regulatory information for “Baxter” Theranova in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e296c5be0d1fd8738783d7618f7f7293 and manufactured by GAMBRO DIALYSATOREN GMBH. The authorized representative in Taiwan is BAXTER HEALTHCARE LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices