gudid
Primary ID: NUF-300
NuForra (UDI NUF-300)
Manufactured by KAIROS BIOSCIENCES LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NuForra - Primary ID NUF-300
Device Regulatory Overview
The NuForra (Model/Catalog Number: NUF-300) is a medical device manufactured by KAIROS BIOSCIENCES LLC. This product is indexed under FDA Product Code / Category Classification KGN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- NUF-300
- Product Code / EMDN
- KGN
- Device Name
- NuForra Surgical Wound Care consists of fibrous, Type I bovine collagen intended for the management of surgical wounds and a wide range of acute and chronic wounds. NuForra is designed to support a moist wound environment to promote natural healing.Indications for Use:Indicated for surgical wounds, partial- and full-thickness wounds, pressure ulcers (Stages I-IV), venous ulcers, ulcers caused by mixed vascular etiologies, venous stasis ulcers, diabetic ulcers, first- and second-degree burns, cuts, and abrasions. NuForra is suitable for application to surgical incision sites and wounds.
- Database Sync Date
- 2026-08-09 09:18:29
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 NuForra?
The registered manufacturer of record for NuForra is KAIROS BIOSCIENCES LLC.
What is the Primary UDI-DI identifier for NuForra?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is NUF-300.
What classification code is assigned to this device?
This device is registered under product classification code KGN.
Similar Classification Devices (KGN)
Other Devices by KAIROS BIOSCIENCES LLC
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