gudid
Primary ID: ITP-005
InteliPowder (UDI ITP-005)
Manufactured by Biogennix, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for InteliPowder - Primary ID ITP-005
Device Regulatory Overview
The InteliPowder (Model/Catalog Number: ITP-005) is a medical device manufactured by Biogennix, LLC. This product is indexed under FDA Product Code / Category Classification KGN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ITP-005
- Product Code / EMDN
- KGN
- Device Name
- InteliPowder Surgical Matrix 5mL
- Database Sync Date
- 2026-08-09 09:04:02
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 InteliPowder?
The registered manufacturer of record for InteliPowder is Biogennix, LLC.
What is the Primary UDI-DI identifier for InteliPowder?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ITP-005.
What classification code is assigned to this device?
This device is registered under product classification code KGN.
Similar Classification Devices (KGN)
Other Devices by Biogennix, LLC
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