eudamed_udi
Primary ID: +D93240011V
Flextray (UDI +D93240011V)
Manufactured by Dent-A-Pharm Produktionsgesellschaft mbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Flextray - Primary ID +D93240011V
Device Regulatory Overview
The Flextray (Model/Catalog Number: 04001) is a medical device manufactured by Dent-A-Pharm Produktionsgesellschaft mbH. This product is indexed under FDA Product Code / Category Classification Q010503 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 04001
- Product Code / EMDN
- Q010503
- Device Name
- Light curing tray material
- Database Sync Date
- 2026-08-09 16:29:18
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 Flextray?
The registered manufacturer of record for Flextray is Dent-A-Pharm Produktionsgesellschaft mbH.
What is the Primary UDI-DI identifier for Flextray?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +D93240011V.
What classification code is assigned to this device?
This device is registered under product classification code Q010503.
Similar Classification Devices (Q010503)
Other Devices by Dent-A-Pharm Produktionsgesellschaft mbH
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint