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APEX Handheld Pulse Oximeter - Indonesia BPOM Medical Device Registration

APEX Handheld Pulse Oximeter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502121887. The device is manufactured by ROSSMAX INNOTEK CORP from Taiwan (China), and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. VASIMITRA NIAGA PERKASA.

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
APEX Handheld Pulse Oximeter
Analysis ID: AKL 20502121887

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Taiwan (China)

Authorized Representative

PT. VASIMITRA NIAGA PERKASA

AR Address

PALMERAH BARAT A4, NO.38

Registration Date

Apr 07, 2021

Expiry Date

Nov 01, 2025

Product Type

Monitoring Cardiology Equipment

Oximeter.

Non Radiation Electromedics

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