eudamed_udi
Primary ID: 07340213302441
Salvelox Dora 20 (UDI 07340213302441)
Manufactured by Orkla Wound Care AB
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Salvelox Dora 20 - Primary ID 07340213302441
Device Regulatory Overview
The Salvelox Dora 20 (Model/Catalog Number: 510005234) is a medical device manufactured by Orkla Wound Care AB. This product is indexed under FDA Product Code / Category Classification M04010102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 510005234
- Product Code / EMDN
- M04010102
- Device Name
- TD 22
- Database Sync Date
- 2026-08-09 16:47:20
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 Salvelox Dora 20?
The registered manufacturer of record for Salvelox Dora 20 is Orkla Wound Care AB.
What is the Primary UDI-DI identifier for Salvelox Dora 20?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07340213302441.
What classification code is assigned to this device?
This device is registered under product classification code M04010102.
Similar Classification Devices (M04010102)
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