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PHILIPS Xper Flex Cardio Physiomonitoring System - Indonesia BPOM Medical Device Registration

PHILIPS Xper Flex Cardio Physiomonitoring System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502512831. The device is manufactured by PHILIPS MEDICAL SYSTEMS. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PHILIPS INDONESIA COMMERCIAL.

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BPOM Registered
Risk Class Kelas Resiko : B
PHILIPS Xper Flex Cardio Physiomonitoring System
Analysis ID: AKL 20502512831

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

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

Jun 08, 2026

Product Type

Monitoring Cardiology Equipment

Cardiac monitor (including cardiotachometer and rate alarm).

Non Radiation Electromedics

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