gudid
Primary ID: 9600169000
CA430 (UDI 9600169000)
Manufactured by ESAOTE SPA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CA430 - Primary ID 9600169000
Device Regulatory Overview
The CA430 (Model/Catalog Number: 9600169000) 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
- 9600169000
- 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 CA430?
The registered manufacturer of record for CA430 is ESAOTE SPA.
What is the Primary UDI-DI identifier for CA430?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 9600169000.
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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