MR 5300 - Indonesia BPOM Medical Device Registration
MR 5300 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501420172. 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 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
PHILIPS INDONESIA COMMERCIALAR Address
Gedung Cibis Nine Lantai 10, Jl. TB Simatupang No. 2
Registration Date
Mar 25, 2024
Expiry Date
Feb 16, 2028
Product Type
Diagnostic Radiology Equipment
Magnetic resonance diagnostic device.
Non Radiation Electromedics
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