Waterpik PowerPulse

FDA UDI

Class I (US FDA UDI)

by Water Pik, Inc.

Identity

Trade Name: Waterpik PowerPulse FDA UDI
Generic Name: External manual massager, home-use FDA UDI
Device Name: Fix mount drencher shower head, chrome FDA UDI
Model / Reference: XMT-633E FDA UDI
Description: Fix mount drencher shower head, chrome FDA UDI

Identifiers

Catalog Number: XMT-633E FDA UDI
Primary DI / UDI-DI: 00073950253710 FDA UDI
FDA Product Code: LYG FDA UDI
GMDN Term: External manual massager, home-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 890.5660 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: External manual massager, home-use

Waterpik PowerPulse by Water Pik, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Water Pik, Inc.

Sources (1)

FDA UDI 8ea2042c-b54a-4397-aeca-bcb2847ffbcf 35 fields · synced May 31, 2026