M22 Laser System - Indonesia BPOM Medical Device Registration
M22 Laser System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603111353. The device is manufactured by LUMENIS (GERMANY) GMBH. from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is SURGIKA ALKESINDO.
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
LUMENIS (GERMANY) GMBH.Country of Origin
Germany
Authorized Representative
SURGIKA ALKESINDOAR Address
Jl. Letjen Suprapto No.60, Gedung Indra Sentral unit G-H, Cempaka Putih
Registration Date
May 08, 2023
Expiry Date
Apr 30, 2026
Product Type
Surgical Equipment
Laser surgical instrument for use in general and plastic surgery and in dermatology.
Non Radiation Electromedics
IDRA – Dedicated Dry Eye Platform
SBM SISTEMI S. R. L
SBM DSLC 200
SBM SISTEMI S.R.L.
SBM DEM 100
SBM SISTEMI S.R.L.
LUMENIS Digital OptiLight System
LUMENIS BE INC.
PLASMAGE
BRERA MEDICAL TECHNOLOGIES S.R.L
LITHOTRIPTER 3000 Plus
RICHARD WOLF GMBH
UFSK Surgeon's Chair surgiForce Light, with Formed Seat
UFSK-INTERNATIONAL OSYS GMBH
LUMENIS Pulse 120H, Moses 2.0
LUMENIS LTD.
MEDTRON ACCUTRON MR
MEDTRON AG.
VERSIUS Surgical System with vLimelite
CMR SURGICAL LIMITED