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ALLPLEX™ Respiratory Panel 1A - Indonesia BPOM Medical Device Registration

ALLPLEX™ Respiratory Panel 1A is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303520055. The device is manufactured by SEEGENE INC. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SCIENCEWERKE.

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BPOM Registered
Risk Class Kelas Resiko : B
ALLPLEX™ Respiratory Panel 1A
Analysis ID: AKL 20303520055

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

SEEGENE INC.

Country of Origin

Korea

Authorized Representative

PT. SCIENCEWERKE

AR Address

Jl.Palmerah Barat No.25

Registration Date

Jan 20, 2025

Expiry Date

Dec 31, 2026

Product Type

Serological Reagents

Respiratory viral panel multiplex nucleic acid assay

Invitro Diagnostics

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