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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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BPOM Registered
Risk Class Kelas Resiko : C
PURIFIER Hollow Fiber Membrane Hemodialyzer
Analysis ID: AKL 20805320828

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

DIAN LANGGENG PRATAMA

AR 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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