PURIFIER Hollow Fiber Membrane Hemodialyzer - Indonesia BPOM Medical Device Registration
PURIFIER Hollow Fiber Membrane Hemodialyzer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805320828. 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 DIAN LANGGENG PRATAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CHENGDU OCI MEDICAL DEVICES CO.,LTDCountry 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
Jul 17, 2023
Expiry Date
Mar 31, 2026
Product Type
Therapeutic Gastroenterology-Urology Equipment
Hemodialysis system and accessories.
Non Electromedic Sterile
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