Pure Global

LIFOTRONIC Shock Wave Therapy System - Indonesia BPOM Medical Device Registration

LIFOTRONIC Shock Wave Therapy System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31403320812. The device is manufactured by SHENZHEN LIFOTRONIC TECHNOLOGY CO., LTD from China, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is LIFOTRONIC TECHNOLOGY 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 : D
LIFOTRONIC Shock Wave Therapy System
Analysis ID: AKL 31403320812

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

China

Authorized Representative

LIFOTRONIC TECHNOLOGY INDONESIA

AR Address

Ruko South Goldfinch Blok SGA No. 17, Jl. Spring Boulevard, Kode Pos 15322, Kel. Cihuni, Kec. Pagedangan, Kab. Tangerang, Provinsi Banten

Registration Date

Oct 25, 2023

Expiry Date

Dec 02, 2025

Product Type

Therapeutic Physical Health Equipment

Extracorporeal shock wave treatment device

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing