StarGuide MDD to MDR Upgrade (UDI 5962426)
Manufactured by G E MEDICAL SYSTEMS ISRAEL LTD.
Device Regulatory Overview
The StarGuide MDD to MDR Upgrade (Model/Catalog Number: 5962426) 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
- 5962426
- Product Code / EMDN
- KPS
- Device Name
- StarGuide SW and Labels Upgrade
- 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 StarGuide MDD to MDR Upgrade?
The registered manufacturer of record for StarGuide MDD to MDR Upgrade is G E MEDICAL SYSTEMS ISRAEL LTD..
What is the Primary UDI-DI identifier for StarGuide MDD to MDR Upgrade?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 5962426.
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.
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