GUDIDData
eudamed_udi Primary ID: 09009607605046

ViVi® FOUR-BAY CHARGER (UDI 09009607605046)

Manufactured by THI Total Healthcare Innovation GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ViVi® FOUR-BAY CHARGER - Primary ID 09009607605046

Device Regulatory Overview

The ViVi® FOUR-BAY CHARGER (Model/Catalog Number: 60504) is a medical device manufactured by THI Total Healthcare Innovation GmbH. This product is indexed under FDA Product Code / Category Classification L0318 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
60504
Product Code / EMDN
L0318
Device Name
ViVi® CHARGER
Database Sync Date
2026-08-09 16:59:56

Full Regulatory Attributes

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{
    "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 ViVi® FOUR-BAY CHARGER?

The registered manufacturer of record for ViVi® FOUR-BAY CHARGER is THI Total Healthcare Innovation GmbH.

What is the Primary UDI-DI identifier for ViVi® FOUR-BAY CHARGER?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 09009607605046.

What classification code is assigned to this device?

This device is registered under product classification code L0318.

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