DCPro-9 Low Flux Polyethersulfone Hollow Fiber Hemodialyzer - Indonesia BPOM Medical Device Registration
DCPro-9 Low Flux Polyethersulfone Hollow Fiber Hemodialyzer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805127744. The device is manufactured by CHENGDU OCI MEDICAL DEVICES CO,LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. DIAN CIPTA PHARMINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CHENGDU OCI MEDICAL DEVICES CO,LTDCountry of Origin
China
Authorized Representative
PT. DIAN CIPTA PHARMINDOAR Address
PURI SENTRA NIAGA JL WIRALOKA NO 44 BLOK B 44-45. CIPINANG MELAYU. JAKARTA TIMUR
Registration Date
Dec 08, 2023
Expiry Date
Dec 07, 2026
Product Type
Therapeutic Gastroenterology-Urology Equipment
Hemodialysis system and accessories.
Non Electromedic Sterile
DCPro-9
SWS HEMODIALYSIS CARE CO., LTD.
DCPro-9 Blood Tubing Set
CHENGDU OCI MEDICAL DEVICES CO., LTD.
DCPro-9 AV Fistula Needles
CHENGDU OCI MEDICAL DEVICES CO., LTD.
DCPro-9 High Flux Polyethersulfone Hollow Fiber Hemodialyzer
CHENGDU OCI MEDICAL DEVICES CO., LTD.

