eudamed_udi
Primary ID: 05711433001551
Thomassplint (UDI 05711433001551)
Manufactured by Sahva A/S
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Thomassplint - Primary ID 05711433001551
Device Regulatory Overview
The Thomassplint (Model/Catalog Number: 14981) is a medical device manufactured by Sahva A/S. This product is indexed under FDA Product Code / Category Classification Y062409,Y062412,Y062415 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 14981
- Product Code / EMDN
- Y062409,Y062412,Y062415
- Device Name
- Thomassplint
- Database Sync Date
- 2026-08-09 18:46:04
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 Thomassplint?
The registered manufacturer of record for Thomassplint is Sahva A/S.
What is the Primary UDI-DI identifier for Thomassplint?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05711433001551.
What classification code is assigned to this device?
This device is registered under product classification code Y062409,Y062412,Y062415.
Similar Classification Devices (Y062409,Y062412,Y062415)
Other Devices by Sahva A/S
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint