eudamed_udi
Primary ID: 00195893754281
Veinlite LEDX (UDI 00195893754281)
Manufactured by Translite, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Veinlite LEDX - Primary ID 00195893754281
Device Regulatory Overview
The Veinlite LEDX (Model/Catalog Number: VLEDX) is a medical device manufactured by Translite, LLC. This product is indexed under FDA Product Code / Category Classification W0202030202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- VLEDX
- Product Code / EMDN
- W0202030202
- Device Name
- Veinlite LEDX
- Database Sync Date
- 2026-08-09 18:14:25
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 Veinlite LEDX?
The registered manufacturer of record for Veinlite LEDX is Translite, LLC.
What is the Primary UDI-DI identifier for Veinlite LEDX?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00195893754281.
What classification code is assigned to this device?
This device is registered under product classification code W0202030202.
Similar Classification Devices (W0202030202)
Other Devices by Translite, LLC
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