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AC 3 OPTIMUS Intra Aortic Balloon Pump (IABP) System - Indonesia BPOM Medical Device Registration

AC 3 OPTIMUS Intra Aortic Balloon Pump (IABP) System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503717179. The device is manufactured by ARROW INTERNATIONAL LLC from United States, and is classified as Risk Class Kelas Resiko : D. 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 : D
AC 3 OPTIMUS Intra Aortic Balloon Pump (IABP) System
Analysis ID: AKL 30503717179

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

United States

Authorized Representative

PT. MULTIDAYA MEDIKA

AR Address

RUKAN NIAGA GUNUNG SAHARI BLOK B-1

Registration Date

Jul 27, 2021

Expiry Date

Dec 31, 2024

Product Type

Prosthetic Cardiology Equipment

Intra-aortic balloon and control system

Non Radiation Electromedics

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