SCHILLER Monitoring System MAGLIFE RT-1 - Indonesia BPOM Medical Device Registration
SCHILLER Monitoring System MAGLIFE RT-1 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502320728. The device is manufactured by SCHILLER MEDICAL SAS from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MULYA HUSADA JAYA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SCHILLER MEDICAL SASCountry of Origin
France
Authorized Representative
MULYA HUSADA JAYAAR Address
JALAN KERINCI NO 2A
Registration Date
Jul 13, 2023
Expiry Date
Oct 31, 2025
Product Type
Monitoring Cardiology Equipment
Cardiac monitor (including cardiotachometer and rate alarm).
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