EUROCOLUMBUS C-Arm Mobile - Indonesia BPOM Medical Device Registration
EUROCOLUMBUS C-Arm Mobile is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501812281. The device is manufactured by EUROCOLUMBUS S.R.L. from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. RAJAWALI MEDIKA MANDIRI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
EUROCOLUMBUS S.R.L.Country of Origin
Italy
Authorized Representative
PT. RAJAWALI MEDIKA MANDIRIAR Address
Jl. Rajawali Sakti Permai B.22-23 RT 08 / RW 01, Kel. Dungus Cariang Kec. Andir Bandung
Registration Date
Nov 08, 2023
Expiry Date
Jul 12, 2028
Product Type
Diagnostic Radiology Equipment
Angiographic x-ray system.
Electromedic Radiation
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