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VIDAMED Defibrillator Monitor - Indonesia BPOM Medical Device Registration

VIDAMED Defibrillator Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30505220060. The device is manufactured by SHENZHEN COMEN MEDICAL INSTRUMENT CO., LTD from China, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. ARIMIA JAYA MANDIRI.

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
VIDAMED Defibrillator Monitor
Analysis ID: AKL 30505220060

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

China

Authorized Representative

PT. ARIMIA JAYA MANDIRI

AR Address

Gedung Konica lantai 3A Jl. Gunung Sahari Raya nomor 78

Registration Date

Jun 10, 2022

Expiry Date

Oct 31, 2026

Product Type

Therapeutic Cardiology Equipment

Automated external defibrillator.

Non Radiation Electromedics

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DJ Fang

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