gudid
Primary ID: 102810020
MyLabTouch (UDI 102810020)
Manufactured by Esaote Europe B.V.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MyLabTouch - Primary ID 102810020
Device Regulatory Overview
The MyLabTouch (Model/Catalog Number: 102810020) is a medical device manufactured by Esaote Europe B.V.. This product is indexed under FDA Product Code / Category Classification IYO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 102810020
- 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 MyLabTouch?
The registered manufacturer of record for MyLabTouch is Esaote Europe B.V..
What is the Primary UDI-DI identifier for MyLabTouch?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 102810020.
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 Europe B.V.
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