gudid
Primary ID: 3330
ClearLook Lighted VersaLoop (UDI 3330)
Manufactured by Bionix, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ClearLook Lighted VersaLoop - Primary ID 3330
Device Regulatory Overview
The ClearLook Lighted VersaLoop (Model/Catalog Number: 3330) 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
- 3330
- Product Code / EMDN
- JYG
- Device Name
- ClearLook Lighted VersaLoop
- 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 ClearLook Lighted VersaLoop?
The registered manufacturer of record for ClearLook Lighted VersaLoop is Bionix, LLC.
What is the Primary UDI-DI identifier for ClearLook Lighted VersaLoop?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 3330.
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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