gudid
Primary ID: 9051-7166
Deltex Medical CardioQ EDM+ (UDI 9051-7166)
Manufactured by DELTEX MEDICAL LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Deltex Medical CardioQ EDM+ - Primary ID 9051-7166
Device Regulatory Overview
The Deltex Medical CardioQ EDM+ (Model/Catalog Number: 9051-7166) is a medical device manufactured by DELTEX MEDICAL LIMITED. This product is indexed under FDA Product Code / Category Classification DPW within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 9051-7166
- Product Code / EMDN
- DPW
- Device Name
- The CardioQ EDM+ is intended for use as a fluid management and cardiac output monitoring system. The system is designed to provide clinicians with real-time information about left-ventricular blood flow.
- Database Sync Date
- 2026-08-09 09:08:18
Full Regulatory Attributes
🔒 Token Gated
{
"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 Deltex Medical CardioQ EDM+?
The registered manufacturer of record for Deltex Medical CardioQ EDM+ is DELTEX MEDICAL LIMITED.
What is the Primary UDI-DI identifier for Deltex Medical CardioQ EDM+?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 9051-7166.
What classification code is assigned to this device?
This device is registered under product classification code DPW.
Similar Classification Devices (DPW)
Other Devices by DELTEX MEDICAL LIMITED
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