GUDIDData
gudid Primary ID: 0998-UC-3013-68

CS100 Intra-Aortic Balloon Pump, Refurbished, PORTUGUESE,NON-UTS,DOM (UDI 0998-UC-3013-68)

Manufactured by Datascope Corp.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CS100 Intra-Aortic Balloon Pump, Refurbished, PORTUGUESE,NON-UTS,DOM - Primary ID 0998-UC-3013-68

Device Regulatory Overview

The CS100 Intra-Aortic Balloon Pump, Refurbished, PORTUGUESE,NON-UTS,DOM (Model/Catalog Number: 0998-UC-3013-68) is a medical device manufactured by Datascope Corp.. This product is indexed under FDA Product Code / Category Classification DSP 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-1486-2026 View Full Alert →

CS100 IABP. Software Version CS100 IABP Q.01....

🔒 Compromised Lot & Serial Numbers Locked
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ID: Z-1487-2026 View Full Alert →

CS300 IABP. Software Version CS300 IABP C.01....

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)
ID: Z-0931-2026 View Full Alert →

Cardiosave Hybrid...

🔒 Compromised Lot & Serial Numbers Locked
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Technical Specifications

Model Number
0998-UC-3013-68
Product Code / EMDN
DSP
Device Name
CS100 Intra-Aortic Balloon Pump, Refurbished, PORTUGUESE,NON-UTS,DOM
Database Sync Date
2026-08-09 09:31:01

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 CS100 Intra-Aortic Balloon Pump, Refurbished, PORTUGUESE,NON-UTS,DOM?

The registered manufacturer of record for CS100 Intra-Aortic Balloon Pump, Refurbished, PORTUGUESE,NON-UTS,DOM is Datascope Corp..

What is the Primary UDI-DI identifier for CS100 Intra-Aortic Balloon Pump, Refurbished, PORTUGUESE,NON-UTS,DOM?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 0998-UC-3013-68.

What classification code is assigned to this device?

This device is registered under product classification code DSP.

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