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KM Intense Pulsed Light Photorejuvenation System - Indonesia BPOM Medical Device Registration

KM Intense Pulsed Light Photorejuvenation System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603912656. The device is manufactured by WEIFANG KM ELECTRONICS CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TRIASA JAYA KENCANA.

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
KM Intense Pulsed Light Photorejuvenation System
Analysis ID: AKL 21603912656

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. TRIASA JAYA KENCANA

AR Address

Jl. Daan Mogot Arcadia KM 22 Blok C2 No. 15 Batu Ceper - Tangerang

Registration Date

Jan 27, 2024

Expiry Date

Dec 20, 2028

Product Type

Surgical Equipment

Laser surgical instrument for use in general and plastic surgery and in dermatology.

Non Radiation Electromedics

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