Taiwan FDA registration 97ce2196852ece2a817ca696843494d4
"Fresenius" multi-filtered blood circuit group pediatric series
TW: "費森尤斯"多重過濾血液迴路組小兒系列
Taiwan·Risk Class 2·FRESENIUS MEDICAL CARE DEUTSCHLAND GMBH ST. WENDEL PLANT·Registered Jan 30, 2007 – Jan 30, 2017CancelledRegistration details
- Analysis ID
- 97ce2196852ece2a817ca696843494d4
- Customs Code
- DHA00601774002
Company information
- Manufacturer Country
- Germany
- Authorized Representative
- FRESENIUS MEDICAL CARE TAIWAN CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.5540 Blood Access Devices and Accessories
- Import Information
- import
Dates and status
- Registration Date
- Jan 30, 2007
- Expiry Date
- Jan 30, 2017
- Cancellation Date
- Dec 20, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Fresenius" multi-filtered blood circuit group pediatric series in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 97ce2196852ece2a817ca696843494d4 and manufactured by FRESENIUS MEDICAL CARE DEUTSCHLAND GMBH ST. WENDEL PLANT. The authorized representative in Taiwan is FRESENIUS MEDICAL CARE TAIWAN CO., 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