LightStim Elipsa - Indonesia BPOM Medical Device Registration
LightStim Elipsa is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21604420038. The device is manufactured by HYDRAFACIAL, LLC from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is BERJAYA AESTHETIC 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.
Risk Classification
Product Class
Kelas : 2
Manufacturer
HYDRAFACIAL, LLCCountry of Origin
United States
Authorized Representative
BERJAYA AESTHETIC INDONESIAAR Address
Jl. Tanah Abang IV Lt. 4 No.34B
Registration Date
Nov 15, 2024
Expiry Date
Jul 26, 2027
Product Type
Therapeutic Surgical Equipment
Low Level Laser Systems for Aesthetic Use
Non Radiation Electromedics

