eudamed_udi
Primary ID: 06944413847774
Diagnostic Ultrasound System (UDI 06944413847774)
Manufactured by Edan Instruments,Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Diagnostic Ultrasound System - Primary ID 06944413847774
Device Regulatory Overview
The Diagnostic Ultrasound System (Model/Catalog Number: Acclarix LX88S) is a medical device manufactured by Edan Instruments,Inc.. This product is indexed under FDA Product Code / Category Classification Z11040101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Acclarix LX88S
- Product Code / EMDN
- Z11040101
- Device Name
- Diagnostic Ultrasound System
- Database Sync Date
- 2026-08-09 16:29:26
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Diagnostic Ultrasound System?
The registered manufacturer of record for Diagnostic Ultrasound System is Edan Instruments,Inc..
What is the Primary UDI-DI identifier for Diagnostic Ultrasound System?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06944413847774.
What classification code is assigned to this device?
This device is registered under product classification code Z11040101.
Similar Classification Devices (Z11040101)
Other Devices by Edan Instruments,Inc.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint