GUDIDData
gudid Primary ID: Control unit arm

Accessories (UDI Control unit arm)

Manufactured by LivaNova Deutschland GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Accessories - Primary ID Control unit arm

Device Regulatory Overview

The Accessories (Model/Catalog Number: Control unit arm) 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
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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
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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
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Unlock Lot Data ($49)

Technical Specifications

Model Number
Control unit arm
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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Frequently Asked Questions

Who is the primary manufacturer of Accessories?

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

What is the Primary UDI-DI identifier for Accessories?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Control unit arm.

What classification code is assigned to this device?

This device is registered under product classification code DTQ.

Programmatic Export

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

JSON API Endpoint