gudid
Primary ID: 10.801.2030
DYNA-Form (UDI 10.801.2030)
Manufactured by COLLAGEN MATRIX, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DYNA-Form - Primary ID 10.801.2030
Device Regulatory Overview
The DYNA-Form (Model/Catalog Number: 10.801.2030) is a medical device manufactured by COLLAGEN MATRIX, INC.. This product is indexed under FDA Product Code / Category Classification NPL within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 10.801.2030
- Product Code / EMDN
- NPL
- Device Name
- Resorbable Collagen Membrane
- Database Sync Date
- 2026-08-09 09:43:33
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 DYNA-Form?
The registered manufacturer of record for DYNA-Form is COLLAGEN MATRIX, INC..
What is the Primary UDI-DI identifier for DYNA-Form?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10.801.2030.
What classification code is assigned to this device?
This device is registered under product classification code NPL.
Similar Classification Devices (NPL)
Other Devices by COLLAGEN MATRIX, INC.
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