gudid
Primary ID: 111187
Axiom Dual-Sump (UDI 111187)
Manufactured by AXIOM MEDICAL, INCORPORATED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Axiom Dual-Sump - Primary ID 111187
Device Regulatory Overview
The Axiom Dual-Sump (Model/Catalog Number: 111187) 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
- 111187
- Product Code / EMDN
- FEG
- Device Name
- Sump Drain, Three Lumens, Silicone, Small Eye, With Filter
- 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 Dual-Sump?
The registered manufacturer of record for Axiom Dual-Sump is AXIOM MEDICAL, INCORPORATED.
What is the Primary UDI-DI identifier for Axiom Dual-Sump?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 111187.
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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