eudamed_udi
Primary ID: 07310610020484
Salvelox Med Blister Rescue Toes 6 (UDI 07310610020484)
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 Med Blister Rescue Toes 6 - Primary ID 07310610020484
Device Regulatory Overview
The Salvelox Med Blister Rescue Toes 6 (Model/Catalog Number: 51030159) is a medical device manufactured by Orkla Wound Care AB. This product is indexed under FDA Product Code / Category Classification M04040501 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 51030159
- Product Code / EMDN
- M04040501
- Device Name
- TD 64
- Database Sync Date
- 2026-08-09 16:50:24
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 Med Blister Rescue Toes 6?
The registered manufacturer of record for Salvelox Med Blister Rescue Toes 6 is Orkla Wound Care AB.
What is the Primary UDI-DI identifier for Salvelox Med Blister Rescue Toes 6?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07310610020484.
What classification code is assigned to this device?
This device is registered under product classification code M04040501.
Similar Classification Devices (M04040501)
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