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Hydrotherapy Whirlpool

FDA UDI

Class II (US FDA UDI)

by Whitehall Manufacturing Co

Identity

Trade Name
Hydrotherapy Whirlpool FDA UDI
Generic Name
Hydro-massage turbine FDA UDI
Device Name
MOBILE EXTREMITY WHIRLPOOL less turbine` FDA UDI
Model / Reference
E-15-M-0002 FDA UDI
Description
MOBILE EXTREMITY WHIRLPOOL less turbine` FDA UDI

Identifiers

Catalog Number
E-15-M-0002 FDA UDI
Primary DI / UDI-DI
00645724002055 FDA UDI
FDA Product Code
ILJ FDA UDI
GMDN Term
Hydro-massage turbine FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5100 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Hydrotherapy bath/tankHydro-massage turbine

Hydrotherapy Whirlpool by Whitehall Manufacturing Co — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hydro-massage turbine.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Whitehall Manufacturing Co

Sources (1)

  • FDA UDI fc6d8762-947a-4ea2-9134-5969b8ed1d1a 35 fields · synced May 31, 2026