Ci-Ca Dialysate System Multifiltrate - Indonesia BPOM Medical Device Registration
Ci-Ca Dialysate System Multifiltrate is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805220319. 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 PT. FRESENIUS MEDICAL CARE INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
NOVA MED GMBHCountry of Origin
Turkey
Authorized Representative
PT. FRESENIUS MEDICAL CARE INDONESIAAR Address
Tempo Scan Tower Lt.20 JL. HR Rasuna Said Kav 3-4, Kuningan , Jakarta Selatan
Registration Date
May 29, 2024
Expiry Date
Aug 31, 2026
Product Type
Therapeutic Gastroenterology-Urology Equipment
Hemodialysis system and accessories.
Non Electromedic Sterile
MULTIFILTRATE PRO Bloodline
MULTIFILTRATE Dialysate System
MULTIFILTRATE Ci-Ca Cassette
MULTIFILTRATE Substituate System
MULTIFILTRATE MPS Substituate System
MULTIFILTRATE HV-CVVH Substituate Set
MULTIFILTRATE Paed CRRT / SCUF Set
MULTIFILTRATE MIDI AV-Set
FRESENIUS MEDICAL CARE HF Female - Spike Adaptor
FRESENIUS MEDICAL CARE SN-Adapter Luer-Lock
FRESENIUS MEDICAL CARE Acid Concentrate for Bicarbonate Haemodialysis
FRESENIUS MEDICAL CARE PRODUCTION SDN. BHD.
BCM - Body Composition Monitor
FRESENIUS MEDICAL CARE DEUTSCHLAND GMBH
MULTIFILTRATEPRO
FRESENIUS MEDICAL CARE DEUTSCHLAND GMBH
FRESENIUS MEDICAL CARE Tenckhoff-Catheter
FRESENIUS MEDICAL CARE DEUTSCHLAND GMBH
AQUABPLUS
VIVONIC GMBH
CITROSTERIL
FRESENIUS MEDICAL CARE PRODUCTION SDN., BHD.
MULTIFILTRATE Cassette
NOVA MED, LTD.
MULTIFILTRATE Dialysate System
NOVA MED GMBH
MULTIFILTRATE Ci-Ca Cassette
NOVA MED GMBH
FRESENIUS MEDICAL CARE Bloodlines
FRESENIUS MEDICAL CARE (JIANGSU) CO., LTD.