PHILIPS SmartPerfusion - Indonesia BPOM Medical Device Registration

PHILIPS SmartPerfusion is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501911135. The device is manufactured by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. from Netherlands, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PHILIPS INDONESIA COMMERCIAL.

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