gudid
Primary ID: AB1251
Advance Biometrix (UDI AB1251)
Manufactured by Lifesignals, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Advance Biometrix - Primary ID AB1251
Device Regulatory Overview
The Advance Biometrix (Model/Catalog Number: AB1251) 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
- AB1251
- Product Code / EMDN
- DRG
- Device Name
- Wearable Biosensor - ECG Remote Monitoring Biosensor
- Database Sync Date
- 2026-08-09 09:18:04
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 Advance Biometrix?
The registered manufacturer of record for Advance Biometrix is Lifesignals, Inc..
What is the Primary UDI-DI identifier for Advance Biometrix?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is AB1251.
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.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint