gudid Primary ID: 3100-1

EasyOne Pro LAB (UDI 3100-1)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The EasyOne Pro LAB (Model/Catalog Number: 3100-1) is a medical device manufactured by NDD Medizintechnik AG. This product is indexed under FDA Product Code / Category Classification BTY within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 3100-1
Product Code / EMDN: BTY
Device Name
Database Sync Date: 2026-08-09 09:16:13

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 EasyOne Pro LAB?

The registered manufacturer of record for EasyOne Pro LAB is NDD Medizintechnik AG.

What is the Primary UDI-DI identifier for EasyOne Pro LAB?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 3100-1.

What classification code is assigned to this device?

This device is registered under product classification code BTY.

Similar Classification Devices (BTY)

Other Devices by NDD Medizintechnik AG

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