LASERLITH I-DUST - Indonesia BPOM Medical Device Registration
LASERLITH I-DUST is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603713707. The device is manufactured by QUANTA SYSTEM SPA. from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is INDOSOPHA SAKTI.
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
QUANTA SYSTEM SPA.Country of Origin
Italy
Authorized Representative
INDOSOPHA SAKTIAR Address
Jl.Mampang Prapatan Raya No.1
Registration Date
Sep 25, 2022
Expiry Date
Jul 25, 2025
Product Type
Surgical Equipment
Laser surgical instrument for use in general and plastic surgery and in dermatology.
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