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REBEAM - Indonesia BPOM Medical Device Registration

REBEAM is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603912115. The device is manufactured by RUIKD from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. BCS PRIMA 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
REBEAM
Analysis ID: AKL 21603912115

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

RUIKD

Country of Origin

Korea

Authorized Representative

PT. BCS PRIMA INDONESIA

AR Address

Jl. Pondok Kopi Raya Blok A No. 8 RT 009 RW 010

Registration Date

Dec 07, 2021

Expiry Date

Dec 18, 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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