gudid
Primary ID: GEN-13044
Gentell (UDI GEN-13044)
Manufactured by Gentell, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Gentell - Primary ID GEN-13044
Device Regulatory Overview
The Gentell (Model/Catalog Number: GEN-13044) is a medical device manufactured by Gentell, LLC. This product is indexed under FDA Product Code / Category Classification FRO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- GEN-13044
- Product Code / EMDN
- FRO
- Device Name
- GEN13044 Gelling Fiber Ag Dressing 4x4 (10cmx10cm)
- Database Sync Date
- 2026-08-09 09:20:07
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 Gentell?
The registered manufacturer of record for Gentell is Gentell, LLC.
What is the Primary UDI-DI identifier for Gentell?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is GEN-13044.
What classification code is assigned to this device?
This device is registered under product classification code FRO.
Similar Classification Devices (FRO)
Other Devices by Gentell, LLC
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