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BELLAVISTA 1000e Ventilator - Indonesia BPOM Medical Device Registration

BELLAVISTA 1000e Ventilator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403124015. The device is manufactured by TECHNOCOM SYSTEMS SDN., BHD. from Malaysia, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. RAJAWALI NUSINDO.

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 : C
BELLAVISTA 1000e Ventilator
Analysis ID: AKL 20403124015

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Malaysia

Authorized Representative

PT. RAJAWALI NUSINDO

AR Address

Gedung RNI Jl. Denpasar Raya Kav DIII Kuningan Jakarta Selatan

Registration Date

Dec 21, 2023

Expiry Date

Dec 31, 2026

Product Type

Therapeutic Anesthesia Equipment

Continuous ventilator.

Non Radiation Electromedics

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