gudid
Primary ID: 003-NFP
NeoForm Putty (UDI 003-NFP)
Manufactured by Biogennix, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NeoForm Putty - Primary ID 003-NFP
Device Regulatory Overview
The NeoForm Putty (Model/Catalog Number: 003-NFP) is a medical device manufactured by Biogennix, LLC. This product is indexed under FDA Product Code / Category Classification MQV within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 003-NFP
- Product Code / EMDN
- MQV
- Device Name
- NeoForm Putty 3cc
- Database Sync Date
- 2026-08-09 09:43:40
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 NeoForm Putty?
The registered manufacturer of record for NeoForm Putty is Biogennix, LLC.
What is the Primary UDI-DI identifier for NeoForm Putty?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 003-NFP.
What classification code is assigned to this device?
This device is registered under product classification code MQV.
Similar Classification Devices (MQV)
Other Devices by Biogennix, LLC
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