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MATRIX Biofilm Remover - Indonesia BPOM Medical Device Registration

MATRIX Biofilm Remover is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903413130. The device is manufactured by WHITELEY CORPORATION PTY.LTD. from Australia, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEDISON JAYA RAYA.

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
MATRIX Biofilm Remover
Analysis ID: AKL 20903413130

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Australia

Authorized Representative

PT. MEDISON JAYA RAYA

AR Address

JL. KAPT.P. TENDEAN NO.7, MAMPANG PRAPATAN

Registration Date

Jul 19, 2023

Expiry Date

Apr 01, 2026

Product Type

General Hospital Equipment and Other Individuals

Liquid chemical sterilants/high level disinfectants.

Non Electromedic Non Sterile

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