gudid
Primary ID: 3410
ClearLook Lighted AngleLoop, Refill (UDI 3410)
Manufactured by Bionix, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ClearLook Lighted AngleLoop, Refill - Primary ID 3410
Device Regulatory Overview
The ClearLook Lighted AngleLoop, Refill (Model/Catalog Number: 3410) 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
- 3410
- Product Code / EMDN
- JYG
- Device Name
- ClearLook Lighted AngleLoop, 50ct Refill
- 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 AngleLoop, Refill?
The registered manufacturer of record for ClearLook Lighted AngleLoop, Refill is Bionix, LLC.
What is the Primary UDI-DI identifier for ClearLook Lighted AngleLoop, Refill?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 3410.
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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