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Actosed PA Powder - Indonesia BPOM Medical Device Registration

Actosed PA Powder is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10903420938. The device is manufactured by GMBH ACT from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is FIVE ALIGNED DISPOS.

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 : A
Actosed PA Powder
Analysis ID: AKL 10903420938

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

GMBH ACT

Country of Origin

Germany

Authorized Representative

FIVE ALIGNED DISPOS

AR Address

Jl. Pulo Sirih Barat Blok M/15, Jaka Setia, Bekasi 17147

Registration Date

Oct 07, 2024

Expiry Date

Jun 28, 2029

Product Type

General Hospital Equipment and Other Individuals

General purpose cleaning for medical device

Non Electromedic Non Sterile

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