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VIVEST Automated External Defibrillator - Indonesia BPOM Medical Device Registration

VIVEST Automated External Defibrillator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30505320218. The device is manufactured by VIVEST MEDICAL TECHNOLOGY CO.,LTD. from China, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. AMPM HEALTHCARE INDONESIA.

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
VIVEST Automated External Defibrillator
Analysis ID: AKL 30505320218

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

China

Authorized Representative

PT. AMPM HEALTHCARE INDONESIA

AR Address

Jl.Cengkeh Kav.16 No.29-30

Registration Date

Jun 26, 2024

Expiry Date

Jan 05, 2026

Product Type

Therapeutic Cardiology Equipment

Automated external defibrillator.

Non Radiation Electromedics

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