gudid
Primary ID: 999090
Axiom (UDI 999090)
Manufactured by AXIOM MEDICAL, INCORPORATED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Axiom - Primary ID 999090
Device Regulatory Overview
The Axiom (Model/Catalog Number: 999090) 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
- 999090
- Product Code / EMDN
- FEG
- Device Name
- Sump Drain Suture Ring Dual-Sump
- 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?
The registered manufacturer of record for Axiom is AXIOM MEDICAL, INCORPORATED.
What is the Primary UDI-DI identifier for Axiom?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 999090.
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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