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OMRON Ultrasonic Nebulizer - Indonesia BPOM Medical Device Registration

OMRON Ultrasonic Nebulizer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403614669. The device is manufactured by OMRON HEALTHCARE CO., LTD. from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. OMRON HEALTHCARE INDONESIA.

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
OMRON Ultrasonic Nebulizer
Analysis ID: AKL 20403614669

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

PT. OMRON HEALTHCARE INDONESIA

AR Address

MENARA BIDAKARA 2 LT 11 UNIT 1,2 DAN 3, JL. JEND. GATOT SUBROTO KAV. 71-73

Registration Date

May 27, 2024

Expiry Date

Dec 31, 2027

Product Type

Therapeutic Anesthesia Equipment

Nebulizer.

Non Radiation Electromedics

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