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BRAILE BIOMEDICA Arterial Blood Filter - Indonesia BPOM Medical Device Registration

BRAILE BIOMEDICA Arterial Blood Filter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20504420086. The device is manufactured by BRAILE BIOMEDICA INDUSTRIA COMERCIO E REPRESENTACOES LTDA from Brazil, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MULTIDAYA MEDIKA.

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
BRAILE BIOMEDICA Arterial Blood Filter
Analysis ID: AKL 20504420086

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Brazil

Authorized Representative

PT. MULTIDAYA MEDIKA

AR Address

RUKAN NIAGA GUNUNG SAHARI BLOK B-1

Registration Date

Jun 24, 2024

Expiry Date

Feb 01, 2029

Product Type

Surgical Cardiology Equipment

Cardiopulmonary bypass arterial line blood filter.

Non Electromedic Sterile

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