gudid
Primary ID: 22511
Lighted Articulating - Sample (UDI 22511)
Manufactured by Bionix, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Lighted Articulating - Sample - Primary ID 22511
Device Regulatory Overview
The Lighted Articulating - Sample (Model/Catalog Number: 22511) is a medical device manufactured by Bionix, LLC. This product is indexed under FDA Product Code / Category Classification JYG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 22511
- Product Code / EMDN
- JYG
- Device Name
- Lighted Articulating Curette - Sample
- Database Sync Date
- 2026-08-09 09:04:11
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 Lighted Articulating - Sample?
The registered manufacturer of record for Lighted Articulating - Sample is Bionix, LLC.
What is the Primary UDI-DI identifier for Lighted Articulating - Sample?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 22511.
What classification code is assigned to this device?
This device is registered under product classification code JYG.
Similar Classification Devices (JYG)
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