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SURFEX Dry Surface Biofilm Remover and Surface Disinfectant - Indonesia BPOM Medical Device Registration

SURFEX Dry Surface Biofilm Remover and Surface Disinfectant is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903819217. 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
SURFEX Dry Surface Biofilm Remover and Surface Disinfectant
Analysis ID: AKL 20903819217

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

Jun 10, 2021

Expiry Date

Dec 31, 2026

Product Type

General Hospital Equipment and Other Individuals

General purpose disinfectants.

Non Electromedic Non Sterile

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