gudid
Primary ID: X-SCREEN
X-SCREEN (UDI X-SCREEN)
Manufactured by STERYLAB SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for X-SCREEN - Primary ID X-SCREEN
Device Regulatory Overview
The X-SCREEN (Model/Catalog Number: X-SCREEN) is a medical device manufactured by STERYLAB SRL. This product is indexed under FDA Product Code / Category Classification FCG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- X-SCREEN
- Product Code / EMDN
- FCG
- Device Name
- Transparent container for transportation of human samples
- Database Sync Date
- 2026-08-09 09:04:33
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 X-SCREEN?
The registered manufacturer of record for X-SCREEN is STERYLAB SRL.
What is the Primary UDI-DI identifier for X-SCREEN?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is X-SCREEN.
What classification code is assigned to this device?
This device is registered under product classification code FCG.
Similar Classification Devices (FCG)
Other Devices by STERYLAB SRL
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint