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ATLANTAMED Ventilator Diomede - Indonesia BPOM Medical Device Registration

ATLANTAMED Ventilator Diomede is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403321290. The device is manufactured by ATLANTAMED LIMITED from United Kingdom, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. HARLISA TRUE GRACE.

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
ATLANTAMED Ventilator Diomede
Analysis ID: AKL 20403321290

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

ATLANTAMED LIMITED

Country of Origin

United Kingdom

Authorized Representative

PT. HARLISA TRUE GRACE

AR Address

Perum Sedati Permai Jl. Sriti HH-15

Registration Date

May 16, 2023

Expiry Date

Dec 31, 2024

Product Type

Therapeutic Anesthesia Equipment

Continuous ventilator.

Non Radiation Electromedics

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