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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.

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BPOM Registered
Risk Class Kelas Resiko : C
K2 Mobile
Analysis ID: AKL 21603023653

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

HULASER, INC

Country of Origin

Korea

Authorized Representative

ICT WORLDWIDE INDONESIA

AR 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.

Non Radiation Electromedics

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