GUDIDData
Bulk Audit Tool API Access
eudamed_udi Primary ID: D-EMRManagerVK

EMR Manager (UDI D-EMRManagerVK)

Manufactured by VEPRO AG

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EMR Manager - Primary ID D-EMRManagerVK

Device Regulatory Overview

The EMR Manager (Model/Catalog Number: EMR Manager V10) is a medical device manufactured by VEPRO AG. This product is indexed under FDA Product Code / Category Classification V92 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
EMR Manager V10
Product Code / EMDN
V92
Device Name
EMR Manager
Database Sync Date
2026-08-09 16:29:19

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 EMR Manager?

The registered manufacturer of record for EMR Manager is VEPRO AG.

What is the Primary UDI-DI identifier for EMR Manager?

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

What classification code is assigned to this device?

This device is registered under product classification code V92.

Similar Classification Devices (V92)

Other Devices by VEPRO AG

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