AccessGUDID - DEVICE: CONAIR (00074108079503)

GUDID

Device Identifier (DI) Information

Brand Name: CONAIR
Version or Model: FB29
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: CONAIR CORPORATION

Primary DI Number: 00074108079503
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 001661222 *Terms of Use

Device Description: Footbath

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	No
Prescription Use (Rx):	No
Over the Counter (OTC):	Yes
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
36557	Foot bath	A mains electricity (AC-powered) device designed to be filled with water to provide therapeutic heat treatment specifically to the feet. It typically consists of a unit with a wide stable base that stands on the floor and includes a shallow receptacle in the centre for the user to place their feet. It has a heating element with thermostat that heats the water to a selected temperature. Some types may have therapeutic foot massage capabilities. This device is intended to relieve foot pain (e.g., ankle joint pain from sprains), as well as headaches, coughs, and other cold symptoms.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
ISA	Massager, Therapeutic, Electric

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: Yes CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 0c696c7e-a702-4ed9-8a43-e4be8b4dd809
Public Version Date: May 03, 2022
Public Version Number: 1
DI Record Publish Date: April 25, 2022

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
No Package DIs found

Secondary DI

[?]

Issuing Agency [?]	Secondary DI Number
No Secondary DIs found

Unit of Use DI

[?]

Unit of Use DI Number: No Unit of Use DI Numbers Found CLOSE

Direct Marking (DM)

[?]

Device Subject to Direct Marking (DM), but Excepted: No
DM DI Different from Primary DI: No
DM DI Number: None
CLOSE

Production Identifier(s) in UDI

[?]

Lot or Batch Number: No
Serial Number: No
Expiration Date: No
Manufacturing Date: No
Donation Identification Number: No CLOSE

Customer Contact

[?]

No Customer Contact currently defined

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