gudid
Primary ID: X5250
PROCAST (UDI X5250)
Manufactured by Dassiet Oy
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PROCAST - Primary ID X5250
Device Regulatory Overview
The PROCAST (Model/Catalog Number: X5250) is a medical device manufactured by Dassiet Oy. This product is indexed under FDA Product Code / Category Classification ITG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- X5250
- Product Code / EMDN
- ITG
- Device Name
- Database Sync Date
- 2026-08-09 09:24:54
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 PROCAST?
The registered manufacturer of record for PROCAST is Dassiet Oy.
What is the Primary UDI-DI identifier for PROCAST?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is X5250.
What classification code is assigned to this device?
This device is registered under product classification code ITG.
Similar Classification Devices (ITG)
Other Devices by Dassiet Oy
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint