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JUSCHEK COVID-19 Antigen Rapid Test (Nasopharyngeal Swab) - Indonesia BPOM Medical Device Registration

JUSCHEK COVID-19 Antigen Rapid Test (Nasopharyngeal Swab) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303120626. The device is manufactured by ACRO BIOTECH, INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is LANIROS DIAN PHARMA.

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BPOM Registered
Risk Class Kelas Resiko : B
JUSCHEK COVID-19 Antigen Rapid Test (Nasopharyngeal Swab)
Analysis ID: AKL 20303120626

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

ACRO BIOTECH, INC.

Country of Origin

United States

Authorized Representative

LANIROS DIAN PHARMA

AR Address

GEDUNG SATRIO TOWER LT. 22, JL. PROF. DR. SATRIO KAV. C4

Registration Date

Dec 05, 2021

Expiry Date

Jul 30, 2025

Product Type

Serological Reagents

Respiratory viral panel multiplex nucleic acid assay

Invitro Diagnostics

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