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ALTUS OMNI II Touch Screen Patient Monitor - Indonesia BPOM Medical Device Registration

ALTUS OMNI II Touch Screen Patient Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502904038. The device is manufactured by INFINIUM MEDICAL INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DEMKA SAKTI.

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
ALTUS OMNI II Touch Screen Patient Monitor
Analysis ID: AKL 20502904038

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. DEMKA SAKTI

AR Address

Jl. Tanah Abang III No. 19 A - B, Jakarta Pusat

Registration Date

Mar 15, 2024

Expiry Date

Jun 30, 2026

Product Type

Monitoring Cardiology Equipment

Cardiac monitor (including cardiotachometer and rate alarm).

Non Radiation Electromedics

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