gudid
Primary ID: D8
DigiDop (UDI D8)
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 D8
Device Regulatory Overview
The DigiDop (Model/Catalog Number: D8) is a medical device manufactured by NEWMAN MEDICAL LLC. This product is indexed under FDA Product Code / Category Classification JAF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- D8
- Product Code / EMDN
- JAF
- Device Name
- 8MHz vascular probe (probe only)
- 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 D8.
What classification code is assigned to this device?
This device is registered under product classification code JAF.
Similar Classification Devices (JAF)
Other Devices by NEWMAN MEDICAL LLC
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