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LIAISON Light Check 12 - Indonesia BPOM Medical Device Registration

LIAISON Light Check 12 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101221610. The device is manufactured by DIASORIN S.P.A from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BIOMEDIKAL SCIENTIFIC INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
LIAISON Light Check 12
Analysis ID: AKL 20101221610

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

DIASORIN S.P.A

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

Oct 03, 2022

Expiry Date

May 19, 2026

Product Type

Clinical Chemistry Test System

Quality control material (assayed and unassayed) (cair)

Invitro Diagnostics

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