K2 Mobile - Indonesia BPOM Medical Device Registration
K2 Mobile is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603023653. The device is manufactured by HULASER, INC from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is ICT WORLDWIDE 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
HULASER, INCCountry of Origin
Korea
Authorized Representative
ICT WORLDWIDE INDONESIAAR Address
Office 88 Lantai 25 Unit H, Jl. Casablanca Raya Kav. 88
Registration Date
Jul 02, 2020
Expiry Date
May 29, 2025
Product Type
Surgical Equipment
Laser surgical instrument for use in general and plastic surgery and in dermatology.
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