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DIA. CHEMILUX HCV Ab - Indonesia BPOM Medical Device Registration

DIA. CHEMILUX HCV Ab is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30305021485. The device is manufactured by DIA.PRO DIAGNOSTIC BIOPROBES S.R.L. from Italy, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. SAKEFA.

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Risk Class Kelas Resiko : D
DIA. CHEMILUX HCV Ab

DIA.CHEMILUX HCV Ab

Analysis ID: AKL 30305021485

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

Italy

Authorized Representative

PT. SAKEFA

AR Address

Jl. Cireunde Raya No.26 Kel. Cireunde Kec. Ciputat Timur

Registration Date

Mar 26, 2020

Expiry Date

Sep 24, 2024

Product Type

Immunological Test System

Antinuclear antibody immunological test system.

Invitro Diagnostics

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