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MUREX HIV Ag/Ab Combination - Indonesia BPOM Medical Device Registration

MUREX HIV Ag/Ab Combination is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30305220419. The device is manufactured by DIASORIN ITALIA S.P.A UK BRANCH from United Kingdom, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. BIOMEDIKAL SCIENTIFIC INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : D
MUREX HIV Ag/Ab Combination
Analysis ID: AKL 30305220419

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

United Kingdom

Authorized Representative

PT. BIOMEDIKAL SCIENTIFIC INDONESIA

AR Address

18 Office Park 22nd F1 Suite E, F &G, Jalan TB SIMATUPANG 18

Registration Date

Aug 23, 2023

Expiry Date

Sep 27, 2027

Product Type

Immunological Test System

Multiple autoantibodies immunological test system.

Invitro Diagnostics

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