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SCHILLER Electrocardiograph - Indonesia BPOM Medical Device Registration

SCHILLER Electrocardiograph is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502021292. The device is manufactured by SCHILLER AG from Switzerland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MULYA HUSADA JAYA.

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Risk Class Kelas Resiko : B
SCHILLER Electrocardiograph
Analysis ID: AKL 20502021292

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

SCHILLER AG

Country of Origin

Switzerland

Authorized Representative

MULYA HUSADA JAYA

AR Address

JALAN KERINCI NO 2A

Registration Date

Oct 17, 2021

Expiry Date

Sep 14, 2026

Product Type

Monitoring Cardiology Equipment

Electrocardiograph.

Non Radiation Electromedics

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