PURIFIER Polyethersulfone Hollow Fiber Hemodialyzer - Indonesia BPOM Medical Device Registration
PURIFIER Polyethersulfone Hollow Fiber Hemodialyzer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805020527. 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 LANGGENG PRATAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CHENGDU OCI MEDICAL DEVICES CO., LTD.Country of Origin
China
Authorized Representative
PT. DIAN LANGGENG PRATAMAAR Address
Gedung Dinar, Jl. Raden Saleh Raya No. 4 RT.10/RW.01, Kel. Kenari, Kec. Senen. Kota Adm. Jakarta Pusat, Provinsi DKI Jakarta, Kode Pos 10430
Registration Date
Mar 04, 2024
Expiry Date
Jan 31, 2027
Product Type
Therapeutic Gastroenterology-Urology Equipment
High permeability hemodialysis system.
Non Electromedic Sterile
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