eudamed_udi
Primary ID: 08053307590332
VISITOR T30 C-DR (UDI 08053307590332)
Manufactured by Technix S.p.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VISITOR T30 C-DR - Primary ID 08053307590332
Device Regulatory Overview
The VISITOR T30 C-DR (Model/Catalog Number: 4695609300) is a medical device manufactured by Technix S.p.A.. This product is indexed under FDA Product Code / Category Classification Z11039016 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 4695609300
- Product Code / EMDN
- Z11039016
- Device Name
- Mobile radiologic units
- Database Sync Date
- 2026-08-09 16:29:52
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 VISITOR T30 C-DR?
The registered manufacturer of record for VISITOR T30 C-DR is Technix S.p.A..
What is the Primary UDI-DI identifier for VISITOR T30 C-DR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08053307590332.
What classification code is assigned to this device?
This device is registered under product classification code Z11039016.
Similar Classification Devices (Z11039016)
Other Devices by Technix S.p.A.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint