GUDIDData
Bulk Audit Tool API Access
gudid Primary ID: Venous Sensor

B-Capta (UDI Venous Sensor)

Manufactured by LivaNova Deutschland GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for B-Capta - Primary ID Venous Sensor

Device Regulatory Overview

The B-Capta (Model/Catalog Number: Venous Sensor) is a medical device manufactured by LivaNova Deutschland GmbH. 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-0571-2025 View Full Alert →

Essenz HLM (Heart-Lung Machine), REF: 49-00-10, with Software...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
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ID: Z-2440-2020 View Full Alert →

Control Panel REF - 60-02-15: LivaNova SCP Pump Control Panel. REF 60-02-15, IPX2, RxOnly, UDI: 04033817900986...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
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ID: Z-2439-2020 View Full Alert →

Control Panel REF - 60-02-50: LivaNova SCP Pump Control Panel S5/C5. REF 60-02-50, IPX2, RxOnly, UDI: 04033817900993...

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

Technical Specifications

Model Number
Venous Sensor
Product Code / EMDN
DRY
Device Name
Database Sync Date
2026-08-09 09:38:00

Full Regulatory Attributes

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

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Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

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Frequently Asked Questions

Who is the primary manufacturer of B-Capta?

The registered manufacturer of record for B-Capta is LivaNova Deutschland GmbH.

What is the Primary UDI-DI identifier for B-Capta?

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

What classification code is assigned to this device?

This device is registered under product classification code DRY.

Similar Classification Devices (DRY)

Other Devices by LivaNova Deutschland GmbH

Programmatic Export

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

JSON API Endpoint