gudid
Primary ID: 74560
Vericore ZR Pro ML (UDI 74560)
Manufactured by WHIP-MIX CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Vericore ZR Pro ML - Primary ID 74560
Device Regulatory Overview
The Vericore ZR Pro ML (Model/Catalog Number: 74560) is a medical device manufactured by WHIP-MIX CORPORATION. This product is indexed under FDA Product Code / Category Classification EIH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 74560
- Product Code / EMDN
- EIH
- Device Name
- Vericore zirconia blanks are made from pre-sintered zirconium dioxide intended to be used with CAD/CAM or manual milling machines. Vericore zirconia blanks are biocompatible and designed to fabricate;-Zirconia Substructures-Restorations (Including inlays, onlays, and veneers)-Crown Framework in the Anterior and Posterior regions-Bridge Framework in the Anterior and Posterior regions
- Database Sync Date
- 2026-08-09 09:02:01
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Vericore ZR Pro ML?
The registered manufacturer of record for Vericore ZR Pro ML is WHIP-MIX CORPORATION.
What is the Primary UDI-DI identifier for Vericore ZR Pro ML?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 74560.
What classification code is assigned to this device?
This device is registered under product classification code EIH.
Similar Classification Devices (EIH)
Other Devices by WHIP-MIX CORPORATION
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