eudamed_udi
Primary ID: 05600456921789
LUCA (UDI 05600456921789)
Manufactured by Orthos XXI, Unipessoal Lda
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LUCA - Primary ID 05600456921789
Device Regulatory Overview
The LUCA (Model/Catalog Number: 53CN4AFPMJU) is a medical device manufactured by Orthos XXI, Unipessoal Lda. This product is indexed under FDA Product Code / Category Classification Y12030601 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 53CN4AFPMJU
- Product Code / EMDN
- Y12030601
- Device Name
- Auxiliares de Marcha - Canadiana
- Database Sync Date
- 2026-08-09 16:29:00
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 LUCA?
The registered manufacturer of record for LUCA is Orthos XXI, Unipessoal Lda.
What is the Primary UDI-DI identifier for LUCA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05600456921789.
What classification code is assigned to this device?
This device is registered under product classification code Y12030601.
Similar Classification Devices (Y12030601)
Other Devices by Orthos XXI, Unipessoal Lda
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