gudid
Primary ID: DMD1091BLK
Vive Precision (UDI DMD1091BLK)
Manufactured by VIVE HEALTH LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Vive Precision - Primary ID DMD1091BLK
Device Regulatory Overview
The Vive Precision (Model/Catalog Number: DMD1091BLK) is a medical device manufactured by VIVE HEALTH LLC. This product is indexed under FDA Product Code / Category Classification DPS within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DMD1091BLK
- Product Code / EMDN
- DPS
- Device Name
- ECG Monitor
- Database Sync Date
- 2026-08-09 09:12:28
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 Vive Precision?
The registered manufacturer of record for Vive Precision is VIVE HEALTH LLC.
What is the Primary UDI-DI identifier for Vive Precision?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is DMD1091BLK.
What classification code is assigned to this device?
This device is registered under product classification code DPS.
Similar Classification Devices (DPS)
Other Devices by VIVE HEALTH LLC
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