gudid
Primary ID: QMR-863ME
Waterpik PowerPulse with DualDock (UDI QMR-863ME)
Manufactured by WATER PIK, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Waterpik PowerPulse with DualDock - Primary ID QMR-863ME
Device Regulatory Overview
The Waterpik PowerPulse with DualDock (Model/Catalog Number: QMR-863ME) is a medical device manufactured by WATER PIK, INC.. This product is indexed under FDA Product Code / Category Classification LYG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- QMR-863ME
- Product Code / EMDN
- LYG
- Device Name
- Hand held shower head, chrome
- Database Sync Date
- 2026-08-09 09:08:47
Full Regulatory Attributes
🔒 Token Gated
{
"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 Waterpik PowerPulse with DualDock?
The registered manufacturer of record for Waterpik PowerPulse with DualDock is WATER PIK, INC..
What is the Primary UDI-DI identifier for Waterpik PowerPulse with DualDock?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is QMR-863ME.
What classification code is assigned to this device?
This device is registered under product classification code LYG.
Similar Classification Devices (LYG)
Other Devices by WATER PIK, INC.
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