gudid
Primary ID: ELEVLED
EleVision (UDI ELEVLED)
Manufactured by SCHLLY FIBEROPTIC GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EleVision - Primary ID ELEVLED
Device Regulatory Overview
The EleVision (Model/Catalog Number: ELEVLED) is a medical device manufactured by SCHLLY FIBEROPTIC GmbH. This product is indexed under FDA Product Code / Category Classification NTN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ELEVLED
- Product Code / EMDN
- NTN
- Device Name
- EleVision TM LED Light Source
- Database Sync Date
- 2026-08-09 09:17:45
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 EleVision?
The registered manufacturer of record for EleVision is SCHLLY FIBEROPTIC GmbH.
What is the Primary UDI-DI identifier for EleVision?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ELEVLED.
What classification code is assigned to this device?
This device is registered under product classification code NTN.
Similar Classification Devices (NTN)
Other Devices by SCHLLY FIBEROPTIC GmbH
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