gudid
Primary ID: C40XN
Eikon (UDI C40XN)
Manufactured by STRYKER CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Eikon - Primary ID C40XN
Device Regulatory Overview
The Eikon (Model/Catalog Number: C40XN) is a medical device manufactured by STRYKER CORPORATION. This product is indexed under FDA Product Code / Category Classification GAD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- C40XN
- Product Code / EMDN
- GAD
- Device Name
- LT Retractor, 40 mm, Extra Narrow
- Database Sync Date
- 2026-08-09 09:31:28
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 Eikon?
The registered manufacturer of record for Eikon is STRYKER CORPORATION.
What is the Primary UDI-DI identifier for Eikon?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is C40XN.
What classification code is assigned to this device?
This device is registered under product classification code GAD.
Similar Classification Devices (GAD)
Other Devices by STRYKER CORPORATION
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint