eudamed_udi
Primary ID: 05600456910332
Sioux (UDI 05600456910332)
Manufactured by Orthos XXI, Unipessoal Lda
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Sioux - Primary ID 05600456910332
Device Regulatory Overview
The Sioux (Model/Catalog Number: 51CDSI2NO43ED) is a medical device manufactured by Orthos XXI, Unipessoal Lda. This product is indexed under FDA Product Code / Category Classification Y122106 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 51CDSI2NO43ED
- Product Code / EMDN
- Y122106
- Device Name
- Cadeira de Rodas
- Database Sync Date
- 2026-08-09 16:28:44
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 Sioux?
The registered manufacturer of record for Sioux is Orthos XXI, Unipessoal Lda.
What is the Primary UDI-DI identifier for Sioux?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05600456910332.
What classification code is assigned to this device?
This device is registered under product classification code Y122106.
Similar Classification Devices (Y122106)
Other Devices by Orthos XXI, Unipessoal Lda
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