Pure Global

MAG & MORE PowerMAG - Indonesia BPOM Medical Device Registration

MAG & MORE PowerMAG is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003817970. The device is manufactured by MAG & MORE GMBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. IT'S YOUR 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 : B
MAG & MORE PowerMAG
Analysis ID: AKL 21003817970

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

MAG & MORE GMBH.

Country of Origin

Germany

Authorized Representative

PT. IT'S YOUR INDONESIA

AR Address

Jl. Kramat Raya No.60A, Kel. Kwitang, Kec. Senen, Kota Adm. Jakarta Pusat, Provinsi DKI Jakarta. Kode Pos : 10420

Registration Date

Jan 14, 2025

Expiry Date

Dec 31, 2029

Product Type

Therapeutic Neurology Equipment

Cranial electrotheraphy stimulator.

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing