gudid
Primary ID: 0072
DenMat (UDI 0072)
Manufactured by DEN-MAT HOLDINGS, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DenMat - Primary ID 0072
Device Regulatory Overview
The DenMat (Model/Catalog Number: 0072) is a medical device manufactured by DEN-MAT HOLDINGS, LLC. This product is indexed under FDA Product Code / Category Classification JEQ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0072
- Product Code / EMDN
- JEQ
- Device Name
- BRSH TIP HANDLE
- Database Sync Date
- 2026-08-09 09:05:40
Full Regulatory Attributes
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{
"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 DenMat?
The registered manufacturer of record for DenMat is DEN-MAT HOLDINGS, LLC.
What is the Primary UDI-DI identifier for DenMat?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 0072.
What classification code is assigned to this device?
This device is registered under product classification code JEQ.
Similar Classification Devices (JEQ)
Other Devices by DEN-MAT HOLDINGS, LLC
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