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GE Voluson Expert 18 - Indonesia BPOM Medical Device Registration

GE Voluson Expert 18 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501220222. The device is manufactured by GE HEALTHCARE AUSTRIA GMBH AND CO OG from Austria, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GE OPERATIONS INDONESIA.

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
GE Voluson Expert 18
Analysis ID: AKL 21501220222

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Austria

Authorized Representative

PT. GE OPERATIONS INDONESIA

AR Address

South Quarter Tower B, Lt. 18-19, Jl. R.A. Kartini Kav. 8

Registration Date

Dec 30, 2024

Expiry Date

Aug 01, 2028

Product Type

Diagnostic Radiology Equipment

Ultrasonic pulsed doppler imaging system.

Non Radiation Electromedics

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