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Conair

FDA UDI

Class I (US FDA UDI)

by Conair Llc.

Identity

Trade Name
CONAIR FDA UDI
Generic Name
Foot bath FDA UDI
Device Name
Footbath FDA UDI
Model / Reference
FB90 FDA UDI
Description
Footbath FDA UDI

Identifiers

Primary DI / UDI-DI
00074108396860 FDA UDI
FDA Product Code
ISA FDA UDI
GMDN Term
Foot bath 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: Foot bath

Conair by Conair Llc. — Class I — 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
Conair Llc.

Sources (1)

  • FDA UDI e8ea3805-1619-4a24-8936-7c3e58516fd1 33 fields · synced Jun 1, 2026