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MEK Hand Held Pulse Oximeter - Indonesia BPOM Medical Device Registration

MEK Hand Held Pulse Oximeter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502310088. The device is manufactured by MEKICS CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PERMANA PUTRA MANDIRI.

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BPOM Registered
Risk Class Kelas Resiko : B
MEK Hand Held Pulse Oximeter
Analysis ID: AKL 20502310088

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

MEKICS CO., LTD.

Country of Origin

Korea

Authorized Representative

PT. PERMANA PUTRA MANDIRI

AR Address

Taman Mini Pintu II Atas No.9 Jakarta Timur

Registration Date

Sep 23, 2019

Expiry Date

May 15, 2024

Product Type

Monitoring Cardiology Equipment

Oximeter.

Non Radiation Electromedics

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