ProKnow DS - Indonesia BPOM Medical Device Registration
ProKnow DS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501420954. The device is manufactured by ELEKTA SOLUTIONS AB from Sweden, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is ELEKTA MEDICAL SOLUTIONS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ELEKTA SOLUTIONS ABCountry of Origin
Sweden
Authorized Representative
ELEKTA MEDICAL SOLUTIONSAR Address
South Quarter Tower B, Lantai 11 unit B, Jalan R.A Kartini Kavling 8
Registration Date
Dec 30, 2024
Expiry Date
Aug 21, 2029
Product Type
Diagnostic Radiology Equipment
Medical image management and processing system.
Non Radiation Electromedics
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