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REA-PEN PRO - Indonesia BPOM Medical Device Registration

REA-PEN PRO is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603028122. The device is manufactured by SUNWOO GLOBAL from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is REDO MARKETING 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 : B
REA-PEN PRO
Analysis ID: AKL 21603028122

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

SUNWOO GLOBAL

Country of Origin

Korea

Authorized Representative

REDO MARKETING INDONESIA

AR Address

Ruko Renata Jl.Jalur Sutera Timur Blok 1A No. 9 Alam Sutera Kel. Kunciran Kec. Pinang

Registration Date

Jul 27, 2023

Expiry Date

Apr 12, 2026

Product Type

Surgical Equipment

Microneedling Device for Aesthetic Use

Non Radiation Electromedics

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