gudid
Primary ID: 8881030
Avance Solo (UDI 8881030)
Manufactured by Mlnlycke Health Care AB
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Avance Solo - Primary ID 8881030
Device Regulatory Overview
The Avance Solo (Model/Catalog Number: 8881030) is a medical device manufactured by Mlnlycke Health Care AB. This product is indexed under FDA Product Code / Category Classification OMP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 8881030
- Product Code / EMDN
- OMP
- Device Name
- Avance Solo Set with Dressing 10x30cm
- Database Sync Date
- 2026-08-09 09:10:28
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 Avance Solo?
The registered manufacturer of record for Avance Solo is Mlnlycke Health Care AB.
What is the Primary UDI-DI identifier for Avance Solo?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 8881030.
What classification code is assigned to this device?
This device is registered under product classification code OMP.
Similar Classification Devices (OMP)
Other Devices by Mlnlycke Health Care AB
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