GUDIDData
eudamed_udi Primary ID: 00850490007238

VitalPatch (UDI 00850490007238)

Manufactured by VitalConnect, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VitalPatch - Primary ID 00850490007238

Device Regulatory Overview

The VitalPatch (Model/Catalog Number: 3037-01) is a medical device manufactured by VitalConnect, Inc.. This product is indexed under FDA Product Code / Category Classification Z12050803 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
3037-01
Product Code / EMDN
Z12050803
Device Name
VitalPatch
Database Sync Date
2026-08-09 17:17:23

Full Regulatory Attributes

πŸ”’ Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of VitalPatch?

The registered manufacturer of record for VitalPatch is VitalConnect, Inc..

What is the Primary UDI-DI identifier for VitalPatch?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00850490007238.

What classification code is assigned to this device?

This device is registered under product classification code Z12050803.

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