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NESCO Fluorescent Quantitative Detection System - Indonesia BPOM Medical Device Registration

NESCO Fluorescent Quantitative Detection System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20304320173. The device is manufactured by SHANDONG BOHONG GENE TECHNOLOGY CO.,LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. DJUNIAR & DJUNIAR.

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BPOM Registered
Risk Class Kelas Resiko : C
NESCO Fluorescent Quantitative Detection System
Analysis ID: AKL 20304320173

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. DJUNIAR & DJUNIAR

AR Address

KOMPLEK RUKAN MAHKOTA ANCOL BLOK D NO.26,JLR.E MARTADINATA ,Desa/Kelurahan Pademangan Barat, Kec.Pademangan,Kota Adm.Jakarta Utara, Provinsi DKI Jakarta. Kode Pos:14420

Registration Date

Jun 16, 2023

Expiry Date

May 04, 2026

Product Type

Immunology Laboratory Equipment and Reagents

RNA Preanalytical Systems.

Invitro Diagnostics

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