gudid
Primary ID: 64062
NeoGen Plug (UDI 64062)
Manufactured by COLLAGEN MATRIX, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NeoGen Plug - Primary ID 64062
Device Regulatory Overview
The NeoGen Plug (Model/Catalog Number: 64062) is a medical device manufactured by COLLAGEN MATRIX, INC.. This product is indexed under FDA Product Code / Category Classification KGN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 64062
- Product Code / EMDN
- KGN
- Device Name
- Resorbable Wound Dressing
- Database Sync Date
- 2026-08-09 09:22:51
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 NeoGen Plug?
The registered manufacturer of record for NeoGen Plug is COLLAGEN MATRIX, INC..
What is the Primary UDI-DI identifier for NeoGen Plug?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 64062.
What classification code is assigned to this device?
This device is registered under product classification code KGN.
Similar Classification Devices (KGN)
Other Devices by COLLAGEN MATRIX, INC.
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