Pure Global

INSTRAMED Automated External Defibrillator With Manual Function - Indonesia BPOM Medical Device Registration

INSTRAMED Automated External Defibrillator With Manual Function is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30505717988. The device is manufactured by INSTRAMED INDUSTRIA MEDICO HOSPITALAR LTDA from Brazil, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. ALKESTRON SELF-SOURCE.

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : D
INSTRAMED Automated External Defibrillator With Manual Function
Analysis ID: AKL 30505717988

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

Brazil

Authorized Representative

PT. ALKESTRON SELF-SOURCE

AR Address

Komp Ruko Griya Inti Sentosa Jln. Griya Agung Blok O No. 95-96

Registration Date

Feb 15, 2020

Expiry Date

Oct 08, 2024

Product Type

Therapeutic Cardiology Equipment

Automated external defibrillator.

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing