gudid
Primary ID: 102810019
MyLabOne (UDI 102810019)
Manufactured by Esaote Europe B.V.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MyLabOne - Primary ID 102810019
Device Regulatory Overview
The MyLabOne (Model/Catalog Number: 102810019) is a medical device manufactured by Esaote Europe B.V.. This product is indexed under FDA Product Code / Category Classification IYN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 102810019
- Product Code / EMDN
- IYN
- Device Name
- Soft. Version R20
- 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 MyLabOne?
The registered manufacturer of record for MyLabOne is Esaote Europe B.V..
What is the Primary UDI-DI identifier for MyLabOne?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 102810019.
What classification code is assigned to this device?
This device is registered under product classification code IYN.
Similar Classification Devices (IYN)
Other Devices by Esaote Europe B.V.
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