Pure Global

NEUSOFT Medical Angiography X-Ray System - Indonesia BPOM Medical Device Registration

NEUSOFT Medical Angiography X-Ray System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501320802. The device is manufactured by NEUSOFT MEDICAL SYSTEMS CO.,LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. HOSPI MEDIK INDONESIA.

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 : C
NEUSOFT Medical Angiography X-Ray System
Analysis ID: AKL 21501320802

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. HOSPI MEDIK INDONESIA

AR Address

Gedung Indra Sentral Blok E-F Lantai 1-2 Jl. Letjen Suprapto No. 60 Kel. Cempaka Putih Barat Kec. Cempaka Putih, Jakarta Pusat 10520

Registration Date

Feb 22, 2023

Expiry Date

Oct 18, 2026

Product Type

Diagnostic Radiology Equipment

Computed tomography x-ray system.

Electromedic Radiation

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing