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HAOBRO Electro-Magnetic Brain Stimulation Device - Indonesia BPOM Medical Device Registration

HAOBRO Electro-Magnetic Brain Stimulation Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003123396. The device is manufactured by SUZHOU HAOBRO MEDICAL DEVICE CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. AESTHETICS PRO INTERNATIONAL.

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 : B
HAOBRO Electro-Magnetic Brain Stimulation Device
Analysis ID: AKL 21003123396

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. AESTHETICS PRO INTERNATIONAL

AR Address

RUKO SURYA INTI JALAN JEMUR ANDAYANI 50 BLOK D 138-139 SURABAYA

Registration Date

Jun 11, 2021

Expiry Date

Feb 02, 2025

Product Type

Therapeutic Neurology Equipment

Repetitive transcranial magnetic stimulation system

Non Radiation Electromedics

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