GUDIDData
Bulk Audit Tool API Access
gudid Primary ID: COCKPITARM - VARIABLE HEIGHT

Device (UDI COCKPITARM - VARIABLE HEIGHT)

Manufactured by LivaNova Deutschland GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Device - Primary ID COCKPITARM - VARIABLE HEIGHT

Device Regulatory Overview

The Device (Model/Catalog Number: COCKPITARM - VARIABLE HEIGHT) is a medical device manufactured by LivaNova Deutschland GmbH. This product is indexed under FDA Product Code / Category Classification DTQ 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
COCKPITARM - VARIABLE HEIGHT
Product Code / EMDN
DTQ
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 Device?

The registered manufacturer of record for Device is LivaNova Deutschland GmbH.

What is the Primary UDI-DI identifier for Device?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is COCKPITARM - VARIABLE HEIGHT.

What classification code is assigned to this device?

This device is registered under product classification code DTQ.

Similar Classification Devices (DTQ)

Other Devices by LivaNova Deutschland GmbH

Programmatic Export

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

JSON API Endpoint