gudid
Primary ID: E900
Elevare ONE (UDI E900)
Manufactured by Omm Imports Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Elevare ONE - Primary ID E900
Device Regulatory Overview
The Elevare ONE (Model/Catalog Number: E900) is a medical device manufactured by Omm Imports Inc.. This product is indexed under FDA Product Code / Category Classification OHS within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- E900
- Product Code / EMDN
- OHS
- Device Name
- Over the counter red/IR device for the treatment of wrinkles.
- Database Sync Date
- 2026-08-09 09:37:50
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 Elevare ONE?
The registered manufacturer of record for Elevare ONE is Omm Imports Inc..
What is the Primary UDI-DI identifier for Elevare ONE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is E900.
What classification code is assigned to this device?
This device is registered under product classification code OHS.
Similar Classification Devices (OHS)
Other Devices by Omm Imports Inc.
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