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B. BRAUN Haemoselect Filter for Plasma Separation - Indonesia BPOM Medical Device Registration

B. BRAUN Haemoselect Filter for Plasma Separation is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20504210479. The device is manufactured by B. BRAUN AVITUM ITALY S.P.A from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. B. BRAUN MEDICAL INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
B. BRAUN Haemoselect Filter for Plasma Separation
Analysis ID: AKL 20504210479

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Italy

Authorized Representative

PT. B. BRAUN MEDICAL INDONESIA

AR Address

Gedung Tempo Scan Tower Lantai 30, Jl. HR Rasuna Said Kav. 3-4 RT 009 RW 004 Kel. Kuningan Timur, Kec. Setiabudi, Kota Administrasi Jakarta Selatan

Registration Date

Jul 28, 2020

Expiry Date

Nov 30, 2023

Product Type

Surgical Cardiology Equipment

Cardiopulmonary bypass arterial line blood filter.

Invitro Diagnostics

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