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MEDINA Defibrillator - Indonesia BPOM Medical Device Registration

MEDINA Defibrillator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30505027442. The device is manufactured by SHENZHEN COMEN MEDICAL INSTRUMENTS CO., LTD. from China, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is MEDINA TECHNIQUE ALKESINDO.

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
MEDINA Defibrillator
Analysis ID: AKL 30505027442

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

China

Authorized Representative

MEDINA TECHNIQUE ALKESINDO

AR Address

Rukan Puri Mansion Blok A No. 28 Jl. Lingkar Luar Barat

Registration Date

Nov 14, 2023

Expiry Date

Mar 13, 2026

Product Type

Therapeutic Cardiology Equipment

Automated external defibrillator.

Non Radiation Electromedics

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