Pure Global

ANKE MAGNETIC RESONANCE IMAGING SYSTEM - Indonesia BPOM Medical Device Registration

ANKE MAGNETIC RESONANCE IMAGING SYSTEM is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501321221. The device is manufactured by SHENZHEN ANKE HIGH-TECH CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is NATIONAL HARMONY OF INDONESIAN TECHNOLOGY.

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
ANKE MAGNETIC RESONANCE IMAGING SYSTEM
Analysis ID: AKL 21501321221

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

AR Address

Ruko Rich Palace, No.36-40 Blok D5, Jl. Meruya Ilir, Srengseng, Kembangan, Jakarta Barat

Registration Date

Aug 25, 2023

Expiry Date

Apr 10, 2028

Product Type

Diagnostic Radiology Equipment

Magnetic resonance diagnostic device.

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing