gudid
Primary ID: G05481
Maglinte (UDI G05481)
Manufactured by COOK INCORPORATED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Maglinte - Primary ID G05481
Device Regulatory Overview
The Maglinte (Model/Catalog Number: G05481) is a medical device manufactured by COOK INCORPORATED. This product is indexed under FDA Product Code / Category Classification FEG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- G05481
- Product Code / EMDN
- FEG
- Device Name
- Maglinte Decompression Sump/Enteroclysis Balloon Catheter
- Database Sync Date
- 2026-08-09 09:33:23
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 Maglinte?
The registered manufacturer of record for Maglinte is COOK INCORPORATED.
What is the Primary UDI-DI identifier for Maglinte?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is G05481.
What classification code is assigned to this device?
This device is registered under product classification code FEG.
Similar Classification Devices (FEG)
Other Devices by COOK INCORPORATED
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