SPACELABS Patient Monitor - Indonesia BPOM Medical Device Registration
SPACELABS Patient Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502913979. The device is manufactured by SPACELABS HEALTHCARE., INC from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GRAHA ISMAYA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SPACELABS HEALTHCARE., INCCountry of Origin
United States
Authorized Representative
PT. GRAHA ISMAYAAR Address
JALAN SULTAN ISKANDAR MUDA KAV 24
Registration Date
Dec 22, 2022
Expiry Date
Apr 17, 2025
Product Type
Monitoring Cardiology Equipment
Cardiac monitor (including cardiotachometer and rate alarm).
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