eudamed_udi
Primary ID: 07640137480295
Veya Dx 9 (UDI 07640137480295)
Manufactured by Tecan Schweiz AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Veya Dx 9 - Primary ID 07640137480295
Device Regulatory Overview
The Veya Dx 9 (Model/Catalog Number: 30246218) is a medical device manufactured by Tecan Schweiz AG. This product is indexed under FDA Product Code / Category Classification W02079099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 30246218
- Product Code / EMDN
- W02079099
- Device Name
- Veya Dx
- Database Sync Date
- 2026-08-09 17:19:53
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 Veya Dx 9?
The registered manufacturer of record for Veya Dx 9 is Tecan Schweiz AG.
What is the Primary UDI-DI identifier for Veya Dx 9?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07640137480295.
What classification code is assigned to this device?
This device is registered under product classification code W02079099.
Similar Classification Devices (W02079099)
Other Devices by Tecan Schweiz AG
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint