BAIN Hollow Fiber Dialyzer (P Series) - Indonesia BPOM Medical Device Registration
BAIN Hollow Fiber Dialyzer (P Series) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805816942. The device is manufactured by BAIN MEDICAL EQUIPMENT(GUANGZHOU) CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is DIAN LANGGENG PRATAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BAIN MEDICAL EQUIPMENT(GUANGZHOU) CO., LTD.Country of Origin
China
Authorized Representative
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
Nov 21, 2023
Expiry Date
Oct 07, 2026
Product Type
Therapeutic Gastroenterology-Urology Equipment
High permeability hemodialysis system.
Non Electromedic Sterile
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