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MGE Nebulizer - Indonesia BPOM Medical Device Registration

MGE Nebulizer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403010156. The device is manufactured by MG ELECTRIC (COLCHESTER) LIMITED from United Kingdom, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ENSEVAL MEDIKA PRIMA.

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
MGE Nebulizer
Analysis ID: AKL 20403010156

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United Kingdom

Authorized Representative

PT. ENSEVAL MEDIKA PRIMA

AR Address

Jl. Pulolentut No. 12 Kawasan Industri Pulogadung

Registration Date

Jan 30, 2019

Expiry Date

Jan 24, 2024

Product Type

Therapeutic Anesthesia Equipment

Nebulizer.

Non Radiation Electromedics

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