XCELTRAX® REPLACEMENT LINER (UDI 00810084333457)
Manufactured by Span Link International, LLC
Device Regulatory Overview
The XCELTRAX® REPLACEMENT LINER (Model/Catalog Number: 79-95555-1) 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
- 79-95555-1
- Product Code / EMDN
- Y06120601
- Device Name
- MAXTRAX XCEL AIR ROM, ANKLE
- Database Sync Date
- 2026-08-09 16:29:28
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of XCELTRAX® REPLACEMENT LINER?
The registered manufacturer of record for XCELTRAX® REPLACEMENT LINER is Span Link International, LLC.
What is the Primary UDI-DI identifier for XCELTRAX® REPLACEMENT LINER?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00810084333457.
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
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint