Pure Global

ARUMALAB AR 580 Hematology Analyzer - Indonesia BPOM Medical Device Registration

ARUMALAB AR 580 Hematology Analyzer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20205420170. The device is manufactured by GENRUI BIOTECH INC from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ELBA LAB 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : B
ARUMALAB AR 580 Hematology Analyzer
Analysis ID: AKL 20205420170

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

GENRUI BIOTECH INC

Country of Origin

China

Authorized Representative

PT. ELBA LAB MEDIKA

AR Address

GRAHA BUMI INDAH LANTAI II ROOM 2005, JL. RAYA KALIMALANG KAV. AGRARIA NO. 8-0 RT/RW 002/016 KEL. DUREN SAWIT KEC. DUREN SAWIT JAKARTA TIMUR

Registration Date

Sep 12, 2024

Expiry Date

Sep 09, 2027

Product Type

Automatic and Semi-Automatic Hematology Equipment

Automated differential cell counter.

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing