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HAKOMED QMD HELIOS - Indonesia BPOM Medical Device Registration

HAKOMED QMD HELIOS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21604420001. The device is manufactured by HAKOMED ITALIA S.R.L. from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ANUGERAH PRIMA MEDIKA.

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.

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BPOM Registered
Risk Class Kelas Resiko : C
HAKOMED QMD HELIOS
Analysis ID: AKL 21604420001

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Italy

Authorized Representative

PT. ANUGERAH PRIMA MEDIKA

AR Address

ANUGERAH PRIMA MEDIKA

Registration Date

Jan 04, 2024

Expiry Date

Jun 30, 2025

Product Type

Therapeutic Surgical Equipment

Low Level Laser Systems for Aesthetic Use

Non Radiation Electromedics

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