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Pro-Matrix - Indonesia BPOM Medical Device Registration

Pro-Matrix is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10603020439. The device is manufactured by ASTEK INNOVATIONS LIMITED from United Kingdom, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is TRI ANUGERAH JAYA.

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
Pro-Matrix
Analysis ID: AKL 10603020439

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

United Kingdom

Authorized Representative

TRI ANUGERAH JAYA

AR Address

Jl. Raya Pos Pengumben 34 G, RT/RW 002/005

Registration Date

Feb 12, 2020

Expiry Date

Aug 23, 2024

Product Type

Surgical Dental Equipment

Dental hand instrument

Non Electromedic Non Sterile

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