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LIAISON® XL Murex HIV Ab/Ag HT - Indonesia BPOM Medical Device Registration

LIAISON® XL Murex HIV Ab/Ag HT is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30305420626. The device is manufactured by DIASORIN ITALIA S.P.A from Italy, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is BIOMEDIKAL SCIENTIFIC INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : D
LIAISON® XL Murex HIV Ab/Ag HT
Analysis ID: AKL 30305420626

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

Italy

Authorized Representative

BIOMEDIKAL SCIENTIFIC INDONESIA

AR Address

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

Registration Date

Dec 10, 2024

Expiry Date

Sep 27, 2027

Product Type

Immunological Test System

Multiple autoantibodies immunological test system.

Invitro Diagnostics

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