gudid
Primary ID: 870 DR
NMCT (UDI 870 DR)
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 NMCT - Primary ID 870 DR
Device Regulatory Overview
The NMCT (Model/Catalog Number: 870 DR) is a medical device manufactured by G E MEDICAL SYSTEMS ISRAEL LTD.. This product is indexed under FDA Product Code / Category Classification JAK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 870 DR
- Product Code / EMDN
- JAK
- Device Name
- 870 DR NM GANTRY FINAL - NEW ROTOR
- 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 NMCT?
The registered manufacturer of record for NMCT is G E MEDICAL SYSTEMS ISRAEL LTD..
What is the Primary UDI-DI identifier for NMCT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 870 DR.
What classification code is assigned to this device?
This device is registered under product classification code JAK.
Similar Classification Devices (JAK)
Other Devices by G E MEDICAL SYSTEMS ISRAEL LTD.
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