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VANAV Skin Beam - Indonesia BPOM Medical Device Registration

VANAV Skin Beam is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403220129. The device is manufactured by DOCTORS TECH CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MERDIS INTERNATIONAL.

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 : B
VANAV Skin Beam
Analysis ID: AKL 21403220129

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Korea

Authorized Representative

PT. MERDIS INTERNATIONAL

AR Address

Gedung DBS Bank Tower Lt.12, Unit 1202 A. Ciputra World 1 Jl. Prof. Dr. Satrio Kav.3-5, Karet Kuningan, Setiabudi, Jakarta Selatan

Registration Date

Jun 03, 2022

Expiry Date

Oct 28, 2026

Product Type

Therapeutic Physical Health Equipment

Infrared lamp.

Non Radiation Electromedics

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