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PHILIPS Ultrasound System 3300 - Indonesia BPOM Medical Device Registration

PHILIPS Ultrasound System 3300 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501025576. The device is manufactured by NEUSOFT MEDICAL SYSTEM CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. 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 Ultrasound System 3300
Analysis ID: AKL 21501025576

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

Sep 23, 2020

Expiry Date

Jun 21, 2025

Product Type

Diagnostic Radiology Equipment

Ultrasonic pulsed doppler imaging system.

Non Radiation Electromedics

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