beta-POWDER - Indonesia BPOM Medical Device Registration
beta-POWDER is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20605026778. The device is manufactured by BRAINBASE CORPORATION from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is WOORI BIO CORPORA.
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.
ฮฒ-POWDER
Risk Classification
Product Class
Kelas : 2
Manufacturer
BRAINBASE CORPORATIONCountry of Origin
Japan
Authorized Representative
WOORI BIO CORPORAAR Address
KOMPLEK GOLDEN PLAZA FATMAWATI BLOK E-43, JL. RS FATMAWATI NO. 15, JAKARTA SELATAN, DKI JAKARTA 12420
Registration Date
Nov 09, 2020
Expiry Date
Aug 21, 2025
Product Type
Other Dental Equipment
Airbrush.
Non Electromedic Sterile

