GUDIDData
gudid Primary ID: LVA1073STL

Vive (UDI LVA1073STL)

Manufactured by VIVE HEALTH LLC

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Vive - Primary ID LVA1073STL

Device Regulatory Overview

The Vive (Model/Catalog Number: LVA1073STL) is a medical device manufactured by VIVE HEALTH LLC. This product is indexed under FDA Product Code / Category Classification ILC within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
LVA1073STL
Product Code / EMDN
ILC
Device Name
Full Stainless Steel Weighted Utensil Set (4pc)
Database Sync Date
2026-08-09 09:32:54

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 Vive?

The registered manufacturer of record for Vive is VIVE HEALTH LLC.

What is the Primary UDI-DI identifier for Vive?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is LVA1073STL.

What classification code is assigned to this device?

This device is registered under product classification code ILC.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint