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AZURION 3 M15 - Indonesia BPOM Medical Device Registration

AZURION 3 M15 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501122271. The device is manufactured by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. from Netherlands, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. PHILIPS INDONESIA COMMERCIAL.

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 : C
AZURION 3 M15
Analysis ID: AKL 21501122271

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Netherlands

Authorized Representative

PT. PHILIPS INDONESIA COMMERCIAL

AR Address

Gedung Cibis Nine Lantai 10, Jl. TB Simatupang No. 2

Registration Date

Mar 30, 2021

Expiry Date

Feb 10, 2026

Product Type

Diagnostic Radiology Equipment

Image-intensified fluoroscopic x-ray system.

Electromedic Radiation

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