gudid
Primary ID: 111169
Axiom Mills Sump (UDI 111169)
Manufactured by AXIOM MEDICAL, INCORPORATED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Axiom Mills Sump - Primary ID 111169
Device Regulatory Overview
The Axiom Mills Sump (Model/Catalog Number: 111169) is a medical device manufactured by AXIOM MEDICAL, INCORPORATED. This product is indexed under FDA Product Code / Category Classification FEG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 111169
- Product Code / EMDN
- FEG
- Device Name
- Dual Lumen, Mediastinal, Round, Silicone, Open Tip
- Database Sync Date
- 2026-08-09 09:36:12
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 Axiom Mills Sump?
The registered manufacturer of record for Axiom Mills Sump is AXIOM MEDICAL, INCORPORATED.
What is the Primary UDI-DI identifier for Axiom Mills Sump?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 111169.
What classification code is assigned to this device?
This device is registered under product classification code FEG.
Similar Classification Devices (FEG)
Other Devices by AXIOM MEDICAL, INCORPORATED
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