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Affiniti 30 Diagnostic Ultrasound System - Indonesia BPOM Medical Device Registration

Affiniti 30 Diagnostic Ultrasound System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501124386. 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 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
Affiniti 30 Diagnostic Ultrasound System
Analysis ID: AKL 21501124386

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PHILIPS INDONESIA COMMERCIAL

AR Address

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

Registration Date

Jul 21, 2021

Expiry Date

Apr 29, 2025

Product Type

Diagnostic Radiology Equipment

Ultrasonic pulsed doppler imaging system.

Non Radiation Electromedics

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DJ Fang

DJ Fang

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