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MICROLIFE Mesh Nebulizer - Indonesia BPOM Medical Device Registration

MICROLIFE Mesh Nebulizer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403520013. The device is manufactured by SHENZEN BI-RICH MEDICAL DEVICES CO. LIMITED from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is CEKINDO BUSINESS INTERNATIONAL.

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
MICROLIFE Mesh Nebulizer
Analysis ID: AKL 20403520013

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

CEKINDO BUSINESS INTERNATIONAL

AR Address

Gedung Axa Tower Lantai 36, Jalan Profesor Doktor Satrio Kaveling 18

Registration Date

Jan 06, 2025

Expiry Date

Sep 26, 2029

Product Type

Therapeutic Anesthesia Equipment

Medicinal nonventilatory nebulizer (atomizer).

Non Radiation Electromedics

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