eudamed_udi
Primary ID: 05060064276457
Class 2IVSoft BeigeBelow KneeRegularClosed Toe (UDI 05060064276457)
Manufactured by urgo ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Class 2IVSoft BeigeBelow KneeRegularClosed Toe - Primary ID 05060064276457
Device Regulatory Overview
The Class 2IVSoft BeigeBelow KneeRegularClosed Toe (Model/Catalog Number: 558796) is a medical device manufactured by urgo ltd. This product is indexed under FDA Product Code / Category Classification M030405 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 558796
- Product Code / EMDN
- M030405
- Device Name
- Altiven
- Database Sync Date
- 2026-08-09 16:28:55
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 Class 2IVSoft BeigeBelow KneeRegularClosed Toe?
The registered manufacturer of record for Class 2IVSoft BeigeBelow KneeRegularClosed Toe is urgo ltd.
What is the Primary UDI-DI identifier for Class 2IVSoft BeigeBelow KneeRegularClosed Toe?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05060064276457.
What classification code is assigned to this device?
This device is registered under product classification code M030405.
Similar Classification Devices (M030405)
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