MEDIANA M32 Patient Monitor - Indonesia BPOM Medical Device Registration

MEDIANA M32 Patient Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502121479. 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. TWO NI ROHA.

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BPOM Registered

Risk Class Kelas Resiko : B

MEDIANA M32 Patient Monitor

Analysis ID: AKL 20502121479

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

Country of Origin

Korea

Authorized Representative

PT. TWO NI ROHA

AR Address

Satrio Tower Building Lantai 22-24 Jalan Prof. Dr. Kav C4 No 5 Kuningan Timur Setia Budi - Jakarta Selatan 12950

Registration Date

Sep 25, 2021

Expiry Date

Dec 31, 2023

Product Type

Monitoring Cardiology Equipment

Cardiac monitor (including cardiotachometer and rate alarm).

Non Radiation Electromedics

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Other Products from MEDIAN CO.,LTD

Products from the same manufacturer (4 products)

MEDIANA Body Composition Analyzer I50

Kelas Resiko : B

MEDIANA BODY COMPOSITION ANALYZER I30

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MEDIANA Body Composition Analyzer I20

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MEDIANA M50 Patient Monitor

Kelas Resiko : B

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