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MEDIX Nebulisers - Indonesia BPOM Medical Device Registration

MEDIX Nebulisers is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403025872. The device is manufactured by CLEMENT CLARKE INTERNATIONAL, LTD from United Kingdom, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GRAHA ISMAYA.

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
MEDIX Nebulisers
Analysis ID: AKL 20403025872

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United Kingdom

Authorized Representative

PT. GRAHA ISMAYA

AR Address

JALAN SULTAN ISKANDAR MUDA KAV 24

Registration Date

Jun 09, 2022

Expiry Date

Aug 01, 2025

Product Type

Therapeutic Anesthesia Equipment

Nebulizer.

Non Radiation Electromedics

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