gudid
Primary ID: 9806150010
MyLab70 XVision (UDI 9806150010)
Manufactured by ESAOTE SPA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MyLab70 XVision - Primary ID 9806150010
Device Regulatory Overview
The MyLab70 XVision (Model/Catalog Number: 9806150010) is a medical device manufactured by ESAOTE SPA. This product is indexed under FDA Product Code / Category Classification IYO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 9806150010
- Product Code / EMDN
- IYO
- 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 MyLab70 XVision?
The registered manufacturer of record for MyLab70 XVision is ESAOTE SPA.
What is the Primary UDI-DI identifier for MyLab70 XVision?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 9806150010.
What classification code is assigned to this device?
This device is registered under product classification code IYO.
Similar Classification Devices (IYO)
Other Devices by ESAOTE SPA
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