gudid
Primary ID: VWCA2
VitaWave (UDI VWCA2)
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 VWCA2
Device Regulatory Overview
The VitaWave (Model/Catalog Number: VWCA2) is a medical device manufactured by Edwards Lifesciences LLC. This product is indexed under FDA Product Code / Category Classification DQK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- VWCA2
- Product Code / EMDN
- DQK
- Device Name
- VitaWave Plus Finger Cuff
- Database Sync Date
- 2026-08-09 09:04:21
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 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 VWCA2.
What classification code is assigned to this device?
This device is registered under product classification code DQK.
Similar Classification Devices (DQK)
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