eudamed_udi
Primary ID: 08435783606910
Unspecified Brand (UDI 08435783606910)
Manufactured by BADER EUROPE GROUP S.L.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 08435783606910
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: 5/402) is a medical device manufactured by BADER EUROPE GROUP S.L.. This product is indexed under FDA Product Code / Category Classification Q010599 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 5/402
- Product Code / EMDN
- Q010599
- Device Name
- DENTAL INSTRUMENTS
- Database Sync Date
- 2026-08-09 16:30:10
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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is BADER EUROPE GROUP S.L..
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08435783606910.
What classification code is assigned to this device?
This device is registered under product classification code Q010599.
Similar Classification Devices (Q010599)
Other Devices by BADER EUROPE GROUP S.L.
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