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GEA Air Compressing Nebulizer - Indonesia BPOM Medical Device Registration

GEA Air Compressing Nebulizer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403903088. The device is manufactured by JIANGSU YUYUE MEDICAL EQUPMENT & SUPPLY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEGA PRATAMA MEDICALINDO.

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
GEA Air Compressing Nebulizer
Analysis ID: AKL 20403903088

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. MEGA PRATAMA MEDICALINDO

AR Address

Jl. Pluit Raya 133 Blok A.3

Registration Date

Jun 14, 2021

Expiry Date

Jun 14, 2024

Product Type

Therapeutic Anesthesia Equipment

Nebulizer.

Non Radiation Electromedics

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DJ Fang

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