GUDIDData
eudamed_udi Primary ID: 00855778005135

LifeVest Wearable Defibrillator, Model 4000 (UDI 00855778005135)

Manufactured by ZOLL Manufacturing Corporation

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LifeVest Wearable Defibrillator, Model 4000 - Primary ID 00855778005135

Device Regulatory Overview

The LifeVest Wearable Defibrillator, Model 4000 (Model/Catalog Number: 10A1025) is a medical device manufactured by ZOLL Manufacturing Corporation. This product is indexed under FDA Product Code / Category Classification C020480 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
10A1025
Product Code / EMDN
C020480
Device Name
LifeVest Wearable Defibrillator - Electrode Belt
Database Sync Date
2026-08-09 16:59:22

Full Regulatory Attributes

πŸ”’ 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 LifeVest Wearable Defibrillator, Model 4000?

The registered manufacturer of record for LifeVest Wearable Defibrillator, Model 4000 is ZOLL Manufacturing Corporation.

What is the Primary UDI-DI identifier for LifeVest Wearable Defibrillator, Model 4000?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00855778005135.

What classification code is assigned to this device?

This device is registered under product classification code C020480.

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