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.
Risk Classification
Product Class
Kelas : 2
Manufacturer
HAKOMED ITALIA S.R.L.Country of Origin
Italy
Authorized Representative
PT. ANUGERAH PRIMA MEDIKAAR 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

