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Up & Up

FDA UDI

Class II (US FDA UDI)

by Target Corporation

Identity

Trade Name
UP & UP FDA UDI
Generic Name
Foot bath FDA UDI
Device Name
Conair Footbath - FB500TGg FDA UDI
Model / Reference
FB500TG FDA UDI
Description
Conair Footbath - FB500TGg FDA UDI

Identifiers

Primary DI / UDI-DI
00074108400703 FDA UDI
FDA Product Code
IMC FDA UDI
GMDN Term
Foot bath FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5110 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Foot bath

Up & Up by Target Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Foot bath.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Target Corporation

Sources (1)

  • FDA UDI 0504280d-1d88-44ef-89c9-6703385911dd 33 fields · synced May 30, 2026