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therascreen® EGFR Plasma RGQ PCR Kit - Indonesia BPOM Medical Device Registration

therascreen® EGFR Plasma RGQ PCR Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20202125618. The device is manufactured by QIAGEN GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is INODIA.

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BPOM Registered
Risk Class Kelas Resiko : C
therascreen® EGFR Plasma RGQ PCR Kit
Analysis ID: AKL 20202125618

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

QIAGEN GMBH

Country of Origin

Germany

Authorized Representative

INODIA

AR Address

Perkantoran Kedoya Elok Plaza Blok DB no 24, Jalan Panjang, Kebon Jeruk

Registration Date

Sep 13, 2021

Expiry Date

Nov 30, 2025

Product Type

Cell and Tissue Culture Products

Somatic Gene Mutation Detection System

Invitro Diagnostics

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