eudamed_udi
Primary ID: +D748219KN2A10C
Unspecified Brand (UDI +D748219KN2A10C)
Manufactured by BIOTEC S.R.L.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID +D748219KN2A10C
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: 219KN2A1) is a medical device manufactured by BIOTEC S.R.L.. This product is indexed under FDA Product Code / Category Classification Q010299 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 219KN2A1
- Product Code / EMDN
- Q010299
- Device Name
- Abutment
- Database Sync Date
- 2026-08-09 16:29:15
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 BIOTEC S.R.L..
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +D748219KN2A10C.
What classification code is assigned to this device?
This device is registered under product classification code Q010299.
Similar Classification Devices (Q010299)
Other Devices by BIOTEC S.R.L.
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