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HUREV OxiPulse SpO2 Sensor - Indonesia BPOM Medical Device Registration

HUREV OxiPulse SpO2 Sensor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502125439. The device is manufactured by HUREV CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SURGIKA ALKESINDO.

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BPOM Registered
Risk Class Kelas Resiko : B
HUREV OxiPulse SpO2 Sensor
Analysis ID: AKL 20502125439

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

HUREV CO., LTD.

Country of Origin

Korea

Authorized Representative

PT. SURGIKA ALKESINDO

AR Address

Jl. Letjen Suprapto No.60, Gedung Indra Sentral unit G-H, Cempaka Putih

Registration Date

May 16, 2023

Expiry Date

Feb 15, 2026

Product Type

Monitoring Cardiology Equipment

Oximeter.

Non Electromedic Non Sterile

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