eudamed_udi
Primary ID: 07310610020477
Salvequick Med Blister Rescue Mix 6 (UDI 07310610020477)
Manufactured by Orkla Wound Care AB
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Salvequick Med Blister Rescue Mix 6 - Primary ID 07310610020477
Device Regulatory Overview
The Salvequick Med Blister Rescue Mix 6 (Model/Catalog Number: 51030158) 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
- 51030158
- Product Code / EMDN
- M04040501
- Device Name
- TD 64
- Database Sync Date
- 2026-08-09 17:08:38
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 Salvequick Med Blister Rescue Mix 6?
The registered manufacturer of record for Salvequick Med Blister Rescue Mix 6 is Orkla Wound Care AB.
What is the Primary UDI-DI identifier for Salvequick Med Blister Rescue Mix 6?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07310610020477.
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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