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LIAISON® EBNA IgG - Indonesia BPOM Medical Device Registration

LIAISON® EBNA IgG is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303220632. The device is manufactured by DIASORIN ITALIA S.P.A from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. BIOMEDIKAL SCIENTIFIC INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
LIAISON® EBNA IgG
Analysis ID: AKL 20303220632

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Italy

Authorized Representative

PT. BIOMEDIKAL SCIENTIFIC INDONESIA

AR Address

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

Registration Date

Mar 18, 2024

Expiry Date

May 19, 2026

Product Type

Serological Reagents

Epstein-Barr virus serological reagents.

Invitro Diagnostics

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DJ Fang

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