eudamed_udi
Primary ID: 00813110028891
Temporary (UDI 00813110028891)
Manufactured by Bicon, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Temporary - Primary ID 00813110028891
Device Regulatory Overview
The Temporary (Model/Catalog Number: 260-363-745) is a medical device manufactured by Bicon, LLC. This product is indexed under FDA Product Code / Category Classification P010299 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 260-363-745
- Product Code / EMDN
- P010299
- Device Name
- Dental Abutment
- Database Sync Date
- 2026-08-09 16:28:59
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 Temporary?
The registered manufacturer of record for Temporary is Bicon, LLC.
What is the Primary UDI-DI identifier for Temporary?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00813110028891.
What classification code is assigned to this device?
This device is registered under product classification code P010299.
Similar Classification Devices (P010299)
Other Devices by Bicon, LLC
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint