eudamed_udi
Primary ID: 08053307591421
ACCORD DR (UDI 08053307591421)
Manufactured by Technix S.p.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ACCORD DR - Primary ID 08053307591421
Device Regulatory Overview
The ACCORD DR (Model/Catalog Number: ACCORD-DR/BR) is a medical device manufactured by Technix S.p.A.. This product is indexed under FDA Product Code / Category Classification Z11039016 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ACCORD-DR/BR
- Product Code / EMDN
- Z11039016
- Device Name
- Mobile radiologic units
- Database Sync Date
- 2026-08-09 16:59:36
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 ACCORD DR?
The registered manufacturer of record for ACCORD DR is Technix S.p.A..
What is the Primary UDI-DI identifier for ACCORD DR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08053307591421.
What classification code is assigned to this device?
This device is registered under product classification code Z11039016.
Similar Classification Devices (Z11039016)
Other Devices by Technix S.p.A.
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