gudid
Primary ID: 7771610
Salem Sump (UDI 7771610)
Manufactured by Cardinal Health, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Salem Sump - Primary ID 7771610
Device Regulatory Overview
The Salem Sump (Model/Catalog Number: 7771610) is a medical device manufactured by Cardinal Health, Inc.. This product is indexed under FDA Product Code / Category Classification FEG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 7771610
- Product Code / EMDN
- FEG
- Device Name
- Dual Lumen Stomach Tube,Multi-functional Port
- Database Sync Date
- 2026-08-09 09:42:40
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 Salem Sump?
The registered manufacturer of record for Salem Sump is Cardinal Health, Inc..
What is the Primary UDI-DI identifier for Salem Sump?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 7771610.
What classification code is assigned to this device?
This device is registered under product classification code FEG.
Similar Classification Devices (FEG)
Other Devices by Cardinal Health, Inc.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint