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PHILIPS EPIQ 5C Diagnostic Ultrasound System - Indonesia BPOM Medical Device Registration

PHILIPS EPIQ 5C Diagnostic Ultrasound System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501220322. The device is manufactured by PHILIPS HEALTHCARE (SUZHOU) CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PHILIPS INDONESIA COMMERCIAL.

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Risk Class Kelas Resiko : B
PHILIPS EPIQ 5C Diagnostic Ultrasound System
Analysis ID: AKL 21501220322

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. PHILIPS INDONESIA COMMERCIAL

AR Address

Gedung Cibis Nine Lantai 10, Jl. TB Simatupang No. 2

Registration Date

Jul 25, 2022

Expiry Date

Nov 15, 2026

Product Type

Diagnostic Radiology Equipment

Ultrasonic pulsed doppler imaging system.

Non Radiation Electromedics

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