gudid
Primary ID: 830
NM (UDI 830)
Manufactured by G E MEDICAL SYSTEMS ISRAEL LTD.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NM - Primary ID 830
Device Regulatory Overview
The NM (Model/Catalog Number: 830) is a medical device manufactured by G E MEDICAL SYSTEMS ISRAEL LTD.. This product is indexed under FDA Product Code / Category Classification KPS within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 830
- Product Code / EMDN
- KPS
- Device Name
- 830 NM GANTRY FINAL WITH NEW ROTOR - MDR CE
- Database Sync Date
- 2026-08-09 09:14:30
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of NM?
The registered manufacturer of record for NM is G E MEDICAL SYSTEMS ISRAEL LTD..
What is the Primary UDI-DI identifier for NM?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 830.
What classification code is assigned to this device?
This device is registered under product classification code KPS.
Similar Classification Devices (KPS)
Other Devices by G E MEDICAL SYSTEMS ISRAEL LTD.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint