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Waterpik ShowerClean Pro with PowerPulse and PowerJET

FDA UDI

Class I (US FDA UDI)

by Water Pik, Inc.

Identity

Trade Name
Waterpik ShowerClean Pro with PowerPulse and PowerJET FDA UDI
Generic Name
External manual massager, home-use FDA UDI
Device Name
Hand held shower head with PowerPulse and PowerJET, chrome FDA UDI
Model / Reference
QCW-763ME FDA UDI
Description
Hand held shower head with PowerPulse and PowerJET, chrome FDA UDI

Identifiers

Catalog Number
QCW-763ME FDA UDI
Primary DI / UDI-DI
00073950316200 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: External manual massager, home-use

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

Similar devices

Also classified as External manual massager, home-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Water Pik, Inc.

Sources (1)

  • FDA UDI 0a57adf9-636a-40c8-86d4-f25578ad7ba3 35 fields · synced May 30, 2026