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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 20502220316. The device is manufactured by ROSSMAX INNOTEK CORP from 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 20502220316

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. VASIMITRA NIAGA PERKASA

AR Address

Jl. WR Supratman Kav.02 RT.002/RW.004

Registration Date

Jul 02, 2024

Expiry Date

Apr 13, 2027

Product Type

Monitoring Cardiology Equipment

Oximeter.

Non Radiation Electromedics

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