LiKAWAVE ® VARIO 3i - Indonesia BPOM Medical Device Registration
LiKAWAVE ® VARIO 3i is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403520028. The device is manufactured by LIKAMED GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PUSPA PHARMA.
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.
Risk Classification
Product Class
Kelas : 2
Manufacturer
LIKAMED GMBHCountry of Origin
Germany
Authorized Representative
PUSPA PHARMAAR Address
Jl.Kemandoran VIII no.1
Registration Date
Feb 05, 2025
Expiry Date
May 07, 2026
Product Type
Therapeutic Physical Health Equipment
Ultrasound and muscle stimulator for use in applying therapeutic deep heat for selected medical conditions
Non Radiation Electromedics

