GUDIDData
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gudid Primary ID: 550AHCT

CDI Blood Parameter Monitoring System 550 (UDI 550AHCT)

Manufactured by Terumo Cardiovascular Systems Corporation

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CDI Blood Parameter Monitoring System 550 - Primary ID 550AHCT

Device Regulatory Overview

The CDI Blood Parameter Monitoring System 550 (Model/Catalog Number: 550AHCT) is a medical device manufactured by Terumo Cardiovascular Systems Corporation. This product is indexed under FDA Product Code / Category Classification DRY 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-2018-2025 View Full Alert →

CDI OneView System BPM Probe: Cat. No. CDI753 - CDI OneView BPM Probe, Cat. No. CDI753TK - CDI OneView BPM Probe Trial Kit...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)
ID: Z-1492-2025 View Full Alert →

Terumo CDI OneView Monitoring System Hematocrit / Oxygen Saturation Probe, Catalog Number REF CD1754...

🔒 Compromised Lot & Serial Numbers Locked
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ID: Z-1401-2024 View Full Alert →

Cardiovascular Procedure Kits that include High Crack Check Valve PN 205307A Part Number: 6375 16010 62974 65246 66312 66342 66388 ...

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

Technical Specifications

Model Number
550AHCT
Product Code / EMDN
DRY
Device Name
Monitor with one blood parameter module and one H/S Probe.
Database Sync Date
2026-08-09 09:40:40

Full Regulatory Attributes

🔒 Token Gated 
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of CDI Blood Parameter Monitoring System 550?

The registered manufacturer of record for CDI Blood Parameter Monitoring System 550 is Terumo Cardiovascular Systems Corporation.

What is the Primary UDI-DI identifier for CDI Blood Parameter Monitoring System 550?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 550AHCT.

What classification code is assigned to this device?

This device is registered under product classification code DRY.

Similar Classification Devices (DRY)

Other Devices by Terumo Cardiovascular Systems Corporation

Programmatic Export

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

JSON API Endpoint