ADVANCED DIGITAL PORTABLE ULTRASONIC SYSTEM (UDI DUS-6000)
Manufactured by ADVANCED INSTRUMENTATIONS, INC.
Device Regulatory Overview
The ADVANCED DIGITAL PORTABLE ULTRASONIC SYSTEM (Model/Catalog Number: DUS-6000) is a medical device manufactured by ADVANCED INSTRUMENTATIONS, INC.. This product is indexed under FDA Product Code / Category Classification IYO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DUS-6000
- Product Code / EMDN
- IYO
- Device Name
- Database Sync Date
- 2026-08-09 09:03:09
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 ADVANCED DIGITAL PORTABLE ULTRASONIC SYSTEM?
The registered manufacturer of record for ADVANCED DIGITAL PORTABLE ULTRASONIC SYSTEM is ADVANCED INSTRUMENTATIONS, INC..
What is the Primary UDI-DI identifier for ADVANCED DIGITAL PORTABLE ULTRASONIC SYSTEM?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is DUS-6000.
What classification code is assigned to this device?
This device is registered under product classification code IYO.
Similar Classification Devices (IYO)
Other Devices by ADVANCED INSTRUMENTATIONS, INC.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint