GUDIDData
Bulk Audit Tool API Access
eudamed_udi Primary ID: 05060472441331

IntelliSpace Corsium (UDI 05060472441331)

Manufactured by Remote Diagnostic Technologies Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for IntelliSpace Corsium - Primary ID 05060472441331

Device Regulatory Overview

The IntelliSpace Corsium (Model/Catalog Number: 01-2507) is a medical device manufactured by Remote Diagnostic Technologies Ltd.. This product is indexed under FDA Product Code / Category Classification Z1203020282 within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 3 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-1027-2026 View Full Alert →

Philips Tempus Pro Patient Monitor, REF: 00-1004, 00-1007, 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R. USB 2-Channel IBP Module, REF: 01-...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)
ID: Z-2175-2025 View Full Alert →

Inseego USB8 4G Dongle Kit, Part Number: 01-2298, which contains USB Flash Drive, Part Number: 43-2011. The kit is an accessory to the Tempu...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)
ID: Z-1729-2025 View Full Alert →

Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, 00-1007...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)

Technical Specifications

Model Number
01-2507
Product Code / EMDN
Z1203020282
Device Name
IntelliSpace Corsium
Database Sync Date
2026-08-09 16:50:40

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 IntelliSpace Corsium?

The registered manufacturer of record for IntelliSpace Corsium is Remote Diagnostic Technologies Ltd..

What is the Primary UDI-DI identifier for IntelliSpace Corsium?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05060472441331.

What classification code is assigned to this device?

This device is registered under product classification code Z1203020282.

Similar Classification Devices (Z1203020282)

Other Devices by Remote Diagnostic Technologies Ltd.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint