GUDIDData
Bulk Audit Tool API Access
gudid Primary ID: B-Capta VENOUS ONLY

Virtual Kit Number (UDI B-Capta VENOUS ONLY)

Manufactured by LivaNova Deutschland GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Virtual Kit Number - Primary ID B-Capta VENOUS ONLY

Device Regulatory Overview

The Virtual Kit Number (Model/Catalog Number: B-Capta VENOUS ONLY) 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.
Unlock Lot Data ($49)
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.
Unlock Lot Data ($49)
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
B-Capta VENOUS ONLY
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 Virtual Kit Number?

The registered manufacturer of record for Virtual Kit Number is LivaNova Deutschland GmbH.

What is the Primary UDI-DI identifier for Virtual Kit Number?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is B-Capta VENOUS ONLY.

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