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.
Risk Classification
Product Class
Kelas : 3
Manufacturer
BIOPLUS CO., LTD.Country of Origin
Korea
Authorized Representative
PT. MULTIANEKA MITRA PERKASA INDONESIAAR 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

