Fresenius multiFiltrate kit Paed CRRT/SCUF
- Registration number
- DE0018291
- Model name
- Ultraflux AV Paed; multiFiltrate paed CRRT/SCUF Set; multiFiltrate kit Paed CRRT/SCUF
- Model identifier
- 5008231; 5017751; 5039051
- Registration date
- June 27, 2016
- Source update date
- May 02, 2024
- Risk class
- Class C
- Product owner
- Fresenius Medical Care AG
- Registrant / registration holder
- FRESENIUS MEDICAL CARE SINGAPORE PTE. LTD.
Kit for continuous renal replacement. Paed CRRT/SCUF (bloodlines & tubing systems Bloodline/Tubing systems are intended for single use only for extracorporeal blood purification. Ultraflux AV paed-filters are designed for single use in acute dialysis with machine-assisted continuous veno-venous haemofiltration, haemodialysis & haemodiafiltration (CVVH, CVVHD, CVVHDF). The filters are specifically meant for use in infants with a body weight of less than 10kg.
- Product owner address
- Else-Kroner-Str. 1, 61352 Bad Homburg, Germany
- Registrant address
- 250 NORTH BRIDGE ROAD, #05-01, RAFFLES CITY TOWER, Singapore 179101
This page mirrors one row from HSA’s official registered-medical-device workbook. Product owner and registrant are separate published roles; neither is relabeled as the manufacturer. The official NOT_GENERATED value is retained when HSA does not publish a registration number, and the device name remains part of the stable record identity.