eudamed_udi
Primary ID: 05600456985156
Euphoria Plus XXL (UDI 05600456985156)
Manufactured by Orthos XXI, Unipessoal Lda
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Euphoria Plus XXL - Primary ID 05600456985156
Device Regulatory Overview
The Euphoria Plus XXL (Model/Catalog Number: 73CM3EUPLXXL) is a medical device manufactured by Orthos XXI, Unipessoal Lda. This product is indexed under FDA Product Code / Category Classification V08060102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 73CM3EUPLXXL
- Product Code / EMDN
- V08060102
- Device Name
- Cama Hospitalar Elétrica
- Database Sync Date
- 2026-08-09 16:28:57
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 Euphoria Plus XXL?
The registered manufacturer of record for Euphoria Plus XXL is Orthos XXI, Unipessoal Lda.
What is the Primary UDI-DI identifier for Euphoria Plus XXL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05600456985156.
What classification code is assigned to this device?
This device is registered under product classification code V08060102.
Similar Classification Devices (V08060102)
Other Devices by Orthos XXI, Unipessoal Lda
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