eudamed_udi
Primary ID: +EDET024501
Ultraprint-Dental IBT UV 1.000 g (UDI +EDET024501)
Manufactured by DETAX GmbH & Co. KG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Ultraprint-Dental IBT UV 1.000 g - Primary ID +EDET024501
Device Regulatory Overview
The Ultraprint-Dental IBT UV 1.000 g (Model/Catalog Number: 02450) is a medical device manufactured by DETAX GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification Q010499 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 02450
- Product Code / EMDN
- Q010499
- Device Name
- Schienungsmaterial, dental, Zubehör
- Database Sync Date
- 2026-08-09 16:29:07
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 Ultraprint-Dental IBT UV 1.000 g?
The registered manufacturer of record for Ultraprint-Dental IBT UV 1.000 g is DETAX GmbH & Co. KG.
What is the Primary UDI-DI identifier for Ultraprint-Dental IBT UV 1.000 g?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +EDET024501.
What classification code is assigned to this device?
This device is registered under product classification code Q010499.
Similar Classification Devices (Q010499)
Other Devices by DETAX GmbH & Co. KG
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