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CardiAid Public Access Defibrillator - Indonesia BPOM Medical Device Registration

CardiAid Public Access Defibrillator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30505220141. The device is manufactured by CARDIA INTERNATIONAL A/S. from Denmark, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. MAIN COMMERCIAL HOSPI.

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
CardiAid Public Access Defibrillator
Analysis ID: AKL 30505220141

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

Denmark

Authorized Representative

PT. MAIN COMMERCIAL HOSPI

AR Address

JL. TAMAN MEKAR AGUNG NO. 32-33 RT.003-RW.006 KEL. MEKARWANGI, KEC. BOJONGLOA KIDUL - KOTA BANDUNG

Registration Date

Dec 19, 2022

Expiry Date

Sep 13, 2027

Product Type

Therapeutic Cardiology Equipment

Automated external defibrillator.

Non Radiation Electromedics

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