gudid Primary ID: 2000 Primus Fitting Unit Pro

Primus By Auditdata (UDI 2000 Primus Fitting Unit Pro)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Primus By Auditdata (Model/Catalog Number: 2000 Primus Fitting Unit Pro) is a medical device manufactured by Auditdata A/S. This product is indexed under FDA Product Code / Category Classification EWO within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 2000 Primus Fitting Unit Pro
Product Code / EMDN: EWO
Device Name
Database Sync Date: 2026-08-09 09:12:44

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 Primus By Auditdata?

The registered manufacturer of record for Primus By Auditdata is Auditdata A/S.

What is the Primary UDI-DI identifier for Primus By Auditdata?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2000 Primus Fitting Unit Pro.

What classification code is assigned to this device?

This device is registered under product classification code EWO.

Similar Classification Devices (EWO)

Other Devices by Auditdata A/S

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