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The RED BiViDerma III - Indonesia BPOM Medical Device Registration

The RED BiViDerma III is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602420038. The device is manufactured by BIOPLUS CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. MULTIANEKA MITRA PERKASA 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 : D
The RED BiViDerma III
Analysis ID: AKL 31602420038

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

BIOPLUS CO., LTD.

Country of Origin

Korea

AR Address

MULTIANEKA MITRA PERKASA INDONESIA

Registration Date

May 06, 2024

Expiry Date

Dec 01, 2026

Product Type

Prosthetic Surgical Equipment

Dermal filler

Non Electromedic Sterile

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