FRESENIUS Dialysis Fistula Needle - Indonesia BPOM Medical Device Registration
FRESENIUS Dialysis Fistula Needle is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805904111. The device is manufactured by NIPRO CORPORATION LTD from Thailand, 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
NIPRO CORPORATION LTDCountry of Origin
Thailand
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
Jul 21, 2020
Expiry Date
Sep 19, 2024
Product Type
Therapeutic Gastroenterology-Urology Equipment
Blood access device and accessories.
Non Electromedic Sterile
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FRESENIUS MEDICAL CARE PRODUCTION SDN. BHD.
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FRESENIUS MEDICAL CARE DEUTSCHLAND GMBH
MULTIFILTRATEPRO
FRESENIUS MEDICAL CARE DEUTSCHLAND GMBH
FRESENIUS MEDICAL CARE Tenckhoff-Catheter
FRESENIUS MEDICAL CARE DEUTSCHLAND GMBH
CITROSTERIL
FRESENIUS MEDICAL CARE PRODUCTION SDN., BHD.
AQUABPLUS
VIVONIC GMBH
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.

