I.G. Patient Monitor - Indonesia BPOM Medical Device Registration
I.G. Patient Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502713853. The device is manufactured by I.G. MEDICAL TECHNOLOGY AND ELECTRONICS GMBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ANDIARTA MARTA UTAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
I.G. MEDICAL TECHNOLOGY AND ELECTRONICS GMBH.Country of Origin
Germany
Authorized Representative
PT. ANDIARTA MARTA UTAMAAR Address
Pusat Niaga Duta Mas Blok C2 No. 11-12 Jl. RS Fatmawati 39
Registration Date
Feb 05, 2021
Expiry Date
Dec 31, 2023
Product Type
Monitoring Cardiology Equipment
Cardiac monitor (including cardiotachometer and rate alarm).
Non Radiation Electromedics

