eudamed_udi
Primary ID: 04751042630316
VeriLab Express DNA (UDI 04751042630316)
Manufactured by SIA Laboveritas
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VeriLab Express DNA - Primary ID 04751042630316
Device Regulatory Overview
The VeriLab Express DNA (Model/Catalog Number: LVE-0014) is a medical device manufactured by SIA Laboveritas. This product is indexed under FDA Product Code / Category Classification W0105900101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- LVE-0014
- Product Code / EMDN
- W0105900101
- Device Name
- Express DNA
- Database Sync Date
- 2026-08-09 16:48:55
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 VeriLab Express DNA?
The registered manufacturer of record for VeriLab Express DNA is SIA Laboveritas.
What is the Primary UDI-DI identifier for VeriLab Express DNA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04751042630316.
What classification code is assigned to this device?
This device is registered under product classification code W0105900101.
Similar Classification Devices (W0105900101)
Other Devices by SIA Laboveritas
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint