ALTUS OMNI Patient Monitor - Indonesia BPOM Medical Device Registration
ALTUS OMNI Patient Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502010386. The device is manufactured by INFINIUM MEDICAL INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DEMKA SAKTI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
INFINIUM MEDICAL INC.Country of Origin
United States
Authorized Representative
PT. DEMKA SAKTIAR Address
Jl. Tanah Abang III No. 19 A - B, Jakarta Pusat
Registration Date
Mar 27, 2024
Expiry Date
Jun 30, 2026
Product Type
Monitoring Cardiology Equipment
Cardiac monitor (including cardiotachometer and rate alarm).
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