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GENFINE Purifier 32 Automatic Nucleic Acid Extractor - Indonesia BPOM Medical Device Registration

GENFINE Purifier 32 Automatic Nucleic Acid Extractor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20304120360. The device is manufactured by GENFINE BIOTECH (CHANGZHOU) CO., LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is INDOLAB ARTHA MEDIKA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : C
GENFINE Purifier 32 Automatic Nucleic Acid Extractor
Analysis ID: AKL 20304120360

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

INDOLAB ARTHA MEDIKA

AR Address

Komp Ruko Sunter Paradise Tahap II Blok.A4 No.43. Sunter Agung Podomoro

Registration Date

Jan 17, 2021

Expiry Date

Sep 14, 2025

Product Type

Immunology Laboratory Equipment and Reagents

RNA Preanalytical Systems.

Invitro Diagnostics

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DJ Fang

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