gudid
Primary ID: 10-900
MASTER-DENT (UDI 10-900)
Manufactured by DENTONICS INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MASTER-DENT - Primary ID 10-900
Device Regulatory Overview
The MASTER-DENT (Model/Catalog Number: 10-900) is a medical device manufactured by DENTONICS INC. This product is indexed under FDA Product Code / Category Classification EMB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 10-900
- Product Code / EMDN
- EMB
- Device Name
- MASTER-DENT ZOE CEMENT (21g/7.5ml)
- Database Sync Date
- 2026-08-09 09:31:31
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 MASTER-DENT?
The registered manufacturer of record for MASTER-DENT is DENTONICS INC.
What is the Primary UDI-DI identifier for MASTER-DENT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10-900.
What classification code is assigned to this device?
This device is registered under product classification code EMB.
Similar Classification Devices (EMB)
Other Devices by DENTONICS INC
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint