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NELLCOR Portable SpO2 Patient Monitoring System - Indonesia BPOM Medical Device Registration

NELLCOR Portable SpO2 Patient Monitoring System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502714759. The device is manufactured by MEDIAN CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEDTRONIC 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 : B
NELLCOR Portable SpO2 Patient Monitoring System
Analysis ID: AKL 20502714759

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

MEDIAN CO., LTD.

Country of Origin

Korea

Authorized Representative

PT. MEDTRONIC INDONESIA

AR Address

Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda

Registration Date

Apr 21, 2022

Expiry Date

Feb 16, 2027

Product Type

Monitoring Cardiology Equipment

Oximeter.

Non Radiation Electromedics

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