gudid
Primary ID: 122001800
AL2443 (UDI 122001800)
Manufactured by ESAOTE SPA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AL2443 - Primary ID 122001800
Device Regulatory Overview
The AL2443 (Model/Catalog Number: 122001800) 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
- 122001800
- Product Code / EMDN
- ITX
- Device Name
- Database Sync Date
- 2026-08-09 09:04:29
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 AL2443?
The registered manufacturer of record for AL2443 is ESAOTE SPA.
What is the Primary UDI-DI identifier for AL2443?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 122001800.
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
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint