SCHILLER Patient Monitor - Indonesia BPOM Medical Device Registration
SCHILLER Patient Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502213008. 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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Risk Classification
Product Class
Kelas : 2
Manufacturer
SCHILLER AG.Country of Origin
Switzerland
Authorized Representative
PT. MULYA HUSADA JAYAAR Address
JALAN KERINCI NO 2A
Registration Date
Jul 16, 2020
Expiry Date
Dec 01, 2023
Product Type
Monitoring Cardiology Equipment
Cardiac monitor (including cardiotachometer and rate alarm).
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