eudamed_udi
Primary ID: 04260415450029
SF Einzeln Large (UDI 04260415450029)
Manufactured by Nicon-Tec GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SF Einzeln Large - Primary ID 04260415450029
Device Regulatory Overview
The SF Einzeln Large (Model/Catalog Number: SFG2-SLBLK) is a medical device manufactured by Nicon-Tec GmbH. This product is indexed under FDA Product Code / Category Classification Y120380 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SFG2-SLBLK
- Product Code / EMDN
- Y120380
- Device Name
- Safety Foot
- Database Sync Date
- 2026-08-09 16:46:18
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 SF Einzeln Large?
The registered manufacturer of record for SF Einzeln Large is Nicon-Tec GmbH.
What is the Primary UDI-DI identifier for SF Einzeln Large?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260415450029.
What classification code is assigned to this device?
This device is registered under product classification code Y120380.
Similar Classification Devices (Y120380)
Other Devices by Nicon-Tec GmbH
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint