gudid
Primary ID: 5.013
Vivos mRNA (UDI 5.013)
Manufactured by Aurum Group Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Vivos mRNA - Primary ID 5.013
Device Regulatory Overview
The Vivos mRNA (Model/Catalog Number: 5.013) is a medical device manufactured by Aurum Group Ltd. This product is indexed under FDA Product Code / Category Classification LRK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 5.013
- Product Code / EMDN
- LRK
- Device Name
- An intraoral device for the treatment of snoring and mild to moderate obstructive sleep apnea in adults.
- Database Sync Date
- 2026-08-09 09:09:51
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Vivos mRNA?
The registered manufacturer of record for Vivos mRNA is Aurum Group Ltd.
What is the Primary UDI-DI identifier for Vivos mRNA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 5.013.
What classification code is assigned to this device?
This device is registered under product classification code LRK.
Similar Classification Devices (LRK)
Other Devices by Aurum Group Ltd
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint