eudamed_udi
Primary ID: 08056209010144
MorbideX® – Protective cushion Adult (UDI 08056209010144)
Manufactured by BenCorpp Srl
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MorbideX® – Protective cushion Adult - Primary ID 08056209010144
Device Regulatory Overview
The MorbideX® – Protective cushion Adult (Model/Catalog Number: MBX-01) is a medical device manufactured by BenCorpp Srl. This product is indexed under FDA Product Code / Category Classification R030180 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MBX-01
- Product Code / EMDN
- R030180
- Device Name
- MorbideX® - Protective Cushion
- Database Sync Date
- 2026-08-09 16:29:28
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 MorbideX® – Protective cushion Adult?
The registered manufacturer of record for MorbideX® – Protective cushion Adult is BenCorpp Srl.
What is the Primary UDI-DI identifier for MorbideX® – Protective cushion Adult?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08056209010144.
What classification code is assigned to this device?
This device is registered under product classification code R030180.
Similar Classification Devices (R030180)
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