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AMX Navigate - Indonesia BPOM Medical Device Registration

AMX Navigate is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501321207. The device is manufactured by GE MEDICAL SYSTEMS LLC from United States, and is classified as Risk Class Kelas Resiko : C. 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 : C
AMX Navigate
Analysis ID: AKL 21501321207

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. GE OPERATIONS INDONESIA

AR Address

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

Registration Date

Apr 22, 2024

Expiry Date

Jan 11, 2027

Product Type

Diagnostic Radiology Equipment

Mobile x-ray system.

Electromedic Radiation

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