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LIAISON XL - Indonesia BPOM Medical Device Registration

LIAISON XL is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20102220254. The device is manufactured by STRATEC SE from Germany, 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 XL
Analysis ID: AKL 20102220254

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

STRATEC SE

Country of Origin

Germany

Authorized Representative

PT. BIOMEDIKAL SCIENTIFIC INDONESIA

AR Address

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

Registration Date

Feb 19, 2024

Expiry Date

May 19, 2026

Product Type

Clinical Laboratory Equipment

Instrumentation for clinical multiplex test systems.

Invitro Diagnostics

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