GUDIDData
gudid Primary ID: CV-6914

CDI H/S Cuvette 1/4 x 1/4 - Japan (UDI CV-6914)

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 H/S Cuvette 1/4 x 1/4 - Japan - Primary ID CV-6914

Device Regulatory Overview

The CDI H/S Cuvette 1/4 x 1/4 - Japan (Model/Catalog Number: CV-6914) 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
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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.
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Technical Specifications

Model Number
CV-6914
Product Code / EMDN
DRY
Device Name
Database Sync Date
2026-08-09 09:04:18

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 H/S Cuvette 1/4 x 1/4 - Japan?

The registered manufacturer of record for CDI H/S Cuvette 1/4 x 1/4 - Japan is Terumo Cardiovascular Systems Corporation.

What is the Primary UDI-DI identifier for CDI H/S Cuvette 1/4 x 1/4 - Japan?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CV-6914.

What classification code is assigned to this device?

This device is registered under product classification code DRY.

Programmatic Export

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