gudid
Primary ID: 101640001
MyLabSeven LCD 19" (UDI 101640001)
Manufactured by ESAOTE SPA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MyLabSeven LCD 19" - Primary ID 101640001
Device Regulatory Overview
The MyLabSeven LCD 19" (Model/Catalog Number: 101640001) 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
- 101640001
- Product Code / EMDN
- IYO
- 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 MyLabSeven LCD 19"?
The registered manufacturer of record for MyLabSeven LCD 19" is ESAOTE SPA.
What is the Primary UDI-DI identifier for MyLabSeven LCD 19"?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 101640001.
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
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint