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TRUESCOPE® Multi Parameter Patient Monitor - Indonesia BPOM Medical Device Registration

TRUESCOPE® Multi Parameter Patient Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502125316. The device is manufactured by GUANGDONG BIOLIGHT MEDITECH CO.,LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MULYA HUSADA JAYA.

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BPOM Registered
Risk Class Kelas Resiko : B
TRUESCOPE® Multi Parameter Patient Monitor
Analysis ID: AKL 20502125316

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. MULYA HUSADA JAYA

AR Address

JALAN KERINCI NO 2A

Registration Date

Jul 07, 2022

Expiry Date

Dec 31, 2023

Product Type

Monitoring Cardiology Equipment

Electrocardiograph.

Non Radiation Electromedics

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