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SCHILLER ARGUS LCM Plus A Patient Monitoring - Indonesia BPOM Medical Device Registration

SCHILLER ARGUS LCM Plus A Patient Monitoring is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502110606. The device is manufactured by SCHILLER AG. from Switzerland, 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
SCHILLER ARGUS LCM Plus A Patient Monitoring
Analysis ID: AKL 20502110606

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

SCHILLER AG.

Country of Origin

Switzerland

Authorized Representative

PT. MULYA HUSADA JAYA

AR Address

JALAN KERINCI NO 2A

Registration Date

Jun 30, 2020

Expiry Date

May 13, 2025

Product Type

Monitoring Cardiology Equipment

Cardiac monitor (including cardiotachometer and rate alarm).

Non Radiation Electromedics

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