gudid
Primary ID: 3440
ClearLook Lighted FlexLoop, Refill (UDI 3440)
Manufactured by Bionix, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ClearLook Lighted FlexLoop, Refill - Primary ID 3440
Device Regulatory Overview
The ClearLook Lighted FlexLoop, Refill (Model/Catalog Number: 3440) 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
- 3440
- Product Code / EMDN
- JYG
- Device Name
- ClearLook Lighted FlexLoop, 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 FlexLoop, Refill?
The registered manufacturer of record for ClearLook Lighted FlexLoop, Refill is Bionix, LLC.
What is the Primary UDI-DI identifier for ClearLook Lighted FlexLoop, Refill?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 3440.
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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