gudid
Primary ID: 9600163000
LA522E (UDI 9600163000)
Manufactured by ESAOTE SPA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LA522E - Primary ID 9600163000
Device Regulatory Overview
The LA522E (Model/Catalog Number: 9600163000) is a medical device manufactured by ESAOTE SPA. This product is indexed under FDA Product Code / Category Classification ITX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 9600163000
- Product Code / EMDN
- ITX
- Device Name
- Database Sync Date
- 2026-08-09 09:04:29
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 LA522E?
The registered manufacturer of record for LA522E is ESAOTE SPA.
What is the Primary UDI-DI identifier for LA522E?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 9600163000.
What classification code is assigned to this device?
This device is registered under product classification code ITX.
Similar Classification Devices (ITX)
Other Devices by ESAOTE SPA
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