gudid
Primary ID: 701
Silicone for Scar Management (UDI 701)
Manufactured by Gottfried Medical, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Silicone for Scar Management - Primary ID 701
Device Regulatory Overview
The Silicone for Scar Management (Model/Catalog Number: 701) is a medical device manufactured by Gottfried Medical, Inc.. This product is indexed under FDA Product Code / Category Classification MDA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 701
- Product Code / EMDN
- MDA
- Device Name
- Ensil Fabric, 8" x 8"
- Database Sync Date
- 2026-08-09 09:03:52
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 Silicone for Scar Management?
The registered manufacturer of record for Silicone for Scar Management is Gottfried Medical, Inc..
What is the Primary UDI-DI identifier for Silicone for Scar Management?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 701.
What classification code is assigned to this device?
This device is registered under product classification code MDA.
Similar Classification Devices (MDA)
Other Devices by Gottfried Medical, Inc.
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