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DEVILBISS Pulmo-Aide Compressor Nebulizer System - Indonesia BPOM Medical Device Registration

DEVILBISS Pulmo-Aide Compressor Nebulizer System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403024522. The device is manufactured by DEVILBISS HEALTHCARE LLC from United Kingdom, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BINABAKTI NIAGAPERKASA.

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 : B
DEVILBISS Pulmo-Aide Compressor Nebulizer System
Analysis ID: AKL 20403024522

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United Kingdom

Authorized Representative

PT. BINABAKTI NIAGAPERKASA

AR Address

Jl. Kebon Jeruk I No. 32 Taman Sari Jakarta Barat

Registration Date

Nov 28, 2022

Expiry Date

Jun 08, 2025

Product Type

Therapeutic Anesthesia Equipment

Nebulizer.

Non Radiation Electromedics

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