GE CardioDay V2.5 - Indonesia BPOM Medical Device Registration
GE CardioDay V2.5 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501914234. The device is manufactured by GETEMED MEDIZIN- UND INFORMATIONSTECHNIK AG. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GE OPERATIONS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GETEMED MEDIZIN- UND INFORMATIONSTECHNIK AG.Country of Origin
Germany
Authorized Representative
PT. GE OPERATIONS INDONESIAAR Address
South Quarter Tower B, Lantai 18-19 Jl. R.A. Kartini, Kav. 8 Kel. Cilandak Barat, Kec. Cilandak Jakarta Selataran 12430
Registration Date
Jul 11, 2019
Expiry Date
Feb 20, 2024
Product Type
Diagnostic Cardiology Equipment
Programmable diagnostic computer.
Non Radiation Electromedics
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