eudamed_udi
Primary ID: 06973596010620
Neo-Velum Singlet (UDI 06973596010620)
Manufactured by Conlett Technology Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Neo-Velum Singlet - Primary ID 06973596010620
Device Regulatory Overview
The Neo-Velum Singlet (Model/Catalog Number: NV-Singlet) is a medical device manufactured by Conlett Technology Inc. This product is indexed under FDA Product Code / Category Classification M0303010203 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- NV-Singlet
- Product Code / EMDN
- M0303010203
- Device Name
- Neo-Velum
- Database Sync Date
- 2026-08-09 17:04:31
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 Neo-Velum Singlet?
The registered manufacturer of record for Neo-Velum Singlet is Conlett Technology Inc.
What is the Primary UDI-DI identifier for Neo-Velum Singlet?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06973596010620.
What classification code is assigned to this device?
This device is registered under product classification code M0303010203.
Similar Classification Devices (M0303010203)
Other Devices by Conlett Technology Inc
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint