gudid
Primary ID: Navigate
AMX (UDI Navigate)
Manufactured by GE Medical Systems, L.L.C.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AMX - Primary ID Navigate
Device Regulatory Overview
The AMX (Model/Catalog Number: Navigate) is a medical device manufactured by GE Medical Systems, L.L.C.. This product is indexed under FDA Product Code / Category Classification IZL within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Navigate
- Product Code / EMDN
- IZL
- Device Name
- AMX Navigate Designated Medical Device Assembly
- Database Sync Date
- 2026-08-09 09:14:30
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of AMX?
The registered manufacturer of record for AMX is GE Medical Systems, L.L.C..
What is the Primary UDI-DI identifier for AMX?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Navigate.
What classification code is assigned to this device?
This device is registered under product classification code IZL.
Similar Classification Devices (IZL)
Other Devices by GE Medical Systems, L.L.C.
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