gudid
Primary ID: MM1250
MonitorMe (UDI MM1250)
Manufactured by Lifesignals, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MonitorMe - Primary ID MM1250
Device Regulatory Overview
The MonitorMe (Model/Catalog Number: MM1250) is a medical device manufactured by Lifesignals, Inc.. This product is indexed under FDA Product Code / Category Classification DRG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MM1250
- Product Code / EMDN
- DRG
- Device Name
- Wearable Biosensor - ECG Remote Monitoring Biosensor Patch
- Database Sync Date
- 2026-08-09 09:18:04
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 MonitorMe?
The registered manufacturer of record for MonitorMe is Lifesignals, Inc..
What is the Primary UDI-DI identifier for MonitorMe?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is MM1250.
What classification code is assigned to this device?
This device is registered under product classification code DRG.
Similar Classification Devices (DRG)
Other Devices by Lifesignals, Inc.
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