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PHILIPS Holter Software - Indonesia BPOM Medical Device Registration

PHILIPS Holter Software is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501320589. The device is manufactured by PHILIPS NORTH AMERICA LLC from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PHILIPS INDONESIA COMMERCIAL.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : B
PHILIPS Holter Software
Analysis ID: AKL 20501320589

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PHILIPS INDONESIA COMMERCIAL

AR Address

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

Registration Date

Jan 25, 2023

Expiry Date

Sep 01, 2026

Product Type

Diagnostic Cardiology Equipment

Programmable diagnostic computer.

Non Radiation Electromedics

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