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Uroskop Omnia Max - Indonesia BPOM Medical Device Registration

Uroskop Omnia Max is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501612326. The device is manufactured by SIEMENS HEALTHCARE GMBH. from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SIEMENS INDONESIA.

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
Uroskop Omnia Max
Analysis ID: AKL 21501612326

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. SIEMENS INDONESIA

AR Address

Jl. Jend. Ahmad Yani Kav. 67-68

Registration Date

Jul 15, 2021

Expiry Date

Mar 15, 2026

Product Type

Diagnostic Radiology Equipment

Image-intensified fluoroscopic x-ray system.

Electromedic Radiation

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