MatriDerm pluS+ Bi-Layer (UDI 83541-300)
Manufactured by MedSkin Solutions Dr. Suwelack AG
Device Regulatory Overview
The MatriDerm pluS+ Bi-Layer (Model/Catalog Number: 83541-300) is a medical device manufactured by MedSkin Solutions Dr. Suwelack AG. This product is indexed under FDA Product Code / Category Classification KGN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 83541-300
- Product Code / EMDN
- KGN
- Device Name
- Database Sync Date
- 2026-08-09 09:17:45
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 MatriDerm pluS+ Bi-Layer?
The registered manufacturer of record for MatriDerm pluS+ Bi-Layer is MedSkin Solutions Dr. Suwelack AG.
What is the Primary UDI-DI identifier for MatriDerm pluS+ Bi-Layer?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 83541-300.
What classification code is assigned to this device?
This device is registered under product classification code KGN.
Similar Classification Devices (KGN)
Other Devices by MedSkin Solutions Dr. Suwelack AG
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