CombiDiagnost R90 - Indonesia BPOM Medical Device Registration
CombiDiagnost R90 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501028005. The device is manufactured by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. from Netherlands, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. PHILIPS INDONESIA COMMERCIAL.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Country of Origin
Netherlands
Authorized Representative
PT. PHILIPS INDONESIA COMMERCIALAR Address
Gedung Cibis Nine Lantai 10, Jl. TB Simatupang No. 2
Registration Date
Dec 18, 2020
Expiry Date
Jun 12, 2025
Product Type
Diagnostic Radiology Equipment
Image-intensified fluoroscopic x-ray system.
Electromedic Radiation
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