MULTIFILTRATE PRO Bloodline - Indonesia BPOM Medical Device Registration
MULTIFILTRATE PRO Bloodline is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805022989. The device is manufactured by NOVA MED GMBH from Turkey, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is FRESENIUS MEDICAL CARE INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
NOVA MED GMBHCountry of Origin
Turkey
Authorized Representative
FRESENIUS MEDICAL CARE INDONESIAAR Address
Tempo Scan Tower, Lt. 20, Jl. H.R. Rasuna Said Kav. 3-4
Registration Date
Oct 31, 2024
Expiry Date
Dec 05, 2028
Product Type
Therapeutic Gastroenterology-Urology Equipment
Hemodialysis system and accessories.
Non Electromedic Sterile
MULTIFILTRATE Dialysate System
MULTIFILTRATE Ci-Ca Cassette
MULTIFILTRATE Substituate System
Ci-Ca Dialysate System Multifiltrate
MULTIFILTRATE MPS Substituate System
MULTIFILTRATE HV-CVVH Substituate Set
MULTIFILTRATE Paed CRRT / SCUF Set
MULTIFILTRATE MIDI AV-Set
FRESENIUS MEDICAL CARE SN-Adapter Luer-Lock
FRESENIUS MEDICAL CARE HF Female - Spike Adaptor
HELIXONE Dialyser
FRESENIUS MEDICAL CARE DEUTSCHLAND GMBH
FRESENIUS MEDICAL CARE Sodium Citrate 4% w/v
FRESENIUS MEDICAL CARE DEUTSCHLAND GMBH
Ci-Ca Dialysate K2 5000 mL
FRESENIUS MEDICAL CARE DEUTSCHLAND GMBH
FX 80 Classix
FRESENIUS MEDICAL CARE SMAD
ULTRAFLUX EMIC 2
FRESENIUS MEDICAL CARE DEUTSCHLAND GMBH
PLASMAFLUX
FRESENIUS MEDICAL CARE DEUTSCHLAND GMBH
FX Classix
FRESENIUS MEDICAL CARE DEUTSCHLAND GMBH
ULTRAFLUX
FRESENIUS MEDICAL CARE DEUTSCHLAND GMBH
MULTIEFFLUENT Bag 10 L
KABOMED FOR MEDICAL INDUSTRIES COMPANY
SILENCIA Vario System 2
KABOMED FOR MEDICAL INDUSTRIES COMPANY