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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.

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BPOM Registered
Risk Class Kelas Resiko : B
LiKAWAVE ® VARIO 3i
Analysis ID: AKL 21403520028

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

LIKAMED GMBH

Country of Origin

Germany

Authorized Representative

PUSPA PHARMA

AR 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

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