eudamed_udi
Primary ID: 00810084332535
MAXTRAX XCEL, COURTE (UDI 00810084332535)
Manufactured by Span Link International, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MAXTRAX XCEL, COURTE - Primary ID 00810084332535
Device Regulatory Overview
The MAXTRAX XCEL, COURTE (Model/Catalog Number: 82-92-XL) is a medical device manufactured by Span Link International, LLC. This product is indexed under FDA Product Code / Category Classification Y06120601 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 82-92-XL
- Product Code / EMDN
- Y06120601
- Device Name
- MAXTRAX XCEL AIR ROM, ANKLE
- Database Sync Date
- 2026-08-09 16:30:24
Full Regulatory Attributes
đź”’ Token Gated
{
"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 MAXTRAX XCEL, COURTE?
The registered manufacturer of record for MAXTRAX XCEL, COURTE is Span Link International, LLC.
What is the Primary UDI-DI identifier for MAXTRAX XCEL, COURTE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00810084332535.
What classification code is assigned to this device?
This device is registered under product classification code Y06120601.
Similar Classification Devices (Y06120601)
Other Devices by Span Link International, LLC
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