gudid
Primary ID: 83400-300
MatriDerm (UDI 83400-300)
Manufactured by MedSkin Solutions Dr. Suwelack AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MatriDerm - Primary ID 83400-300
Device Regulatory Overview
The MatriDerm (Model/Catalog Number: 83400-300) 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
- 83400-300
- Product Code / EMDN
- KGN
- Device Name
- MatriDerm Large 210 x 297 x 2 mm
- 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?
The registered manufacturer of record for MatriDerm is MedSkin Solutions Dr. Suwelack AG.
What is the Primary UDI-DI identifier for MatriDerm?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 83400-300.
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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