gudid
Primary ID: DD-901-D3W
DigiDop (UDI DD-901-D3W)
Manufactured by NEWMAN MEDICAL LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DigiDop - Primary ID DD-901-D3W
Device Regulatory Overview
The DigiDop (Model/Catalog Number: DD-901-D3W) is a medical device manufactured by NEWMAN MEDICAL LLC. This product is indexed under FDA Product Code / Category Classification LXE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DD-901-D3W
- Product Code / EMDN
- LXE
- Device Name
- DigiDop 901, Table Top Doppler, 3MHZ OB WATERPROOF
- Database Sync Date
- 2026-08-09 09:49:32
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 DigiDop?
The registered manufacturer of record for DigiDop is NEWMAN MEDICAL LLC.
What is the Primary UDI-DI identifier for DigiDop?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is DD-901-D3W.
What classification code is assigned to this device?
This device is registered under product classification code LXE.
Similar Classification Devices (LXE)
Other Devices by NEWMAN MEDICAL LLC
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