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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.

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BPOM Registered
Risk Class Kelas Resiko : C
LightStim Elipsa
Analysis ID: AKL 21604420038

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

HYDRAFACIAL, LLC

Country of Origin

United States

Authorized Representative

BERJAYA AESTHETIC INDONESIA

AR 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

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