gudid
Primary ID: QTL-965MEP
Waterpik PowerPulse with Qwik-Pause (UDI QTL-965MEP)
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 Qwik-Pause - Primary ID QTL-965MEP
Device Regulatory Overview
The Waterpik PowerPulse with Qwik-Pause (Model/Catalog Number: QTL-965MEP) 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
- QTL-965MEP
- Product Code / EMDN
- LYG
- Device Name
- Hand held shower head, black
- 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 Qwik-Pause?
The registered manufacturer of record for Waterpik PowerPulse with Qwik-Pause is WATER PIK, INC..
What is the Primary UDI-DI identifier for Waterpik PowerPulse with Qwik-Pause?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is QTL-965MEP.
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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