gudid
Primary ID: VWCA
VitaWave (UDI VWCA)
Manufactured by Edwards Lifesciences LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VitaWave - Primary ID VWCA
Device Regulatory Overview
The VitaWave (Model/Catalog Number: VWCA) is a medical device manufactured by Edwards Lifesciences LLC. This product is indexed under FDA Product Code / Category Classification DXN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- VWCA
- Product Code / EMDN
- DXN
- Device Name
- VitaWave Finger Cuff Adult
- Database Sync Date
- 2026-08-09 09:04:21
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 VitaWave?
The registered manufacturer of record for VitaWave is Edwards Lifesciences LLC.
What is the Primary UDI-DI identifier for VitaWave?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is VWCA.
What classification code is assigned to this device?
This device is registered under product classification code DXN.
Similar Classification Devices (DXN)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint