gudid
Primary ID: 3000-1
EasyOne Pro (UDI 3000-1)
Manufactured by NDD Medizintechnik AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EasyOne Pro - Primary ID 3000-1
Device Regulatory Overview
The EasyOne Pro (Model/Catalog Number: 3000-1) 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
- 3000-1
- 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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of EasyOne Pro?
The registered manufacturer of record for EasyOne Pro is NDD Medizintechnik AG.
What is the Primary UDI-DI identifier for EasyOne Pro?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 3000-1.
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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