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LKTECH Diode Laser - Indonesia BPOM Medical Device Registration

LKTECH Diode Laser is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21604320039. The device is manufactured by BEIJING SANO LASER S&T DEVELOPMENT, CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. JAMBERDETAK DERMA TECH.

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
LKTECH Diode Laser
Analysis ID: AKL 21604320039

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. JAMBERDETAK DERMA TECH

AR Address

KOMPLEK PAKUAN, Jl. INTAN PAKUAN II NOMOR 2, RT 002 RW 007

Registration Date

Sep 04, 2023

Expiry Date

Sep 01, 2026

Product Type

Therapeutic Surgical Equipment

Low Level Laser Systems for Aesthetic Use

Non Radiation Electromedics

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