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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.

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BPOM Registered
Risk Class Kelas Resiko : B
beta-POWDER

ฮฒ-POWDER

Analysis ID: AKL 20605026778

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

WOORI BIO CORPORA

AR 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

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