Pure Global

MAGSTIM 200 Magnetic Stimulator - Indonesia BPOM Medical Device Registration

MAGSTIM 200 Magnetic Stimulator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003320129. The device is manufactured by THE MAGSTIM COMPANY LTD. from United Kingdom, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. KARINDO ALKESTRON.

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
MAGSTIM 200 Magnetic Stimulator
Analysis ID: AKL 21003320129

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United Kingdom

Authorized Representative

PT. KARINDO ALKESTRON

AR Address

JL. TOMANG RAYA NO.17

Registration Date

Jun 06, 2023

Expiry Date

Nov 29, 2027

Product Type

Therapeutic Neurology Equipment

External functional neuromuscular stimulator.

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing