gudid
Primary ID: 531512
ProBase (UDI 531512)
Manufactured by IVOCLAR VIVADENT AKTIENGESELLSCHAFT
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ProBase - Primary ID 531512
Device Regulatory Overview
The ProBase (Model/Catalog Number: 531512) is a medical device manufactured by IVOCLAR VIVADENT AKTIENGESELLSCHAFT. This product is indexed under FDA Product Code / Category Classification EBI within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 531512
- Product Code / EMDN
- EBI
- Device Name
- denture base materials
- Database Sync Date
- 2026-08-09 09:01:09
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 ProBase?
The registered manufacturer of record for ProBase is IVOCLAR VIVADENT AKTIENGESELLSCHAFT.
What is the Primary UDI-DI identifier for ProBase?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 531512.
What classification code is assigned to this device?
This device is registered under product classification code EBI.
Similar Classification Devices (EBI)
Other Devices by IVOCLAR VIVADENT AKTIENGESELLSCHAFT
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint