AccessGUDID - DEVICE: SuperPole™ FRS Floor Receptacle (00689281005050)

GUDID

Device Identifier (DI) Information

Brand Name: SuperPole™ FRS Floor Receptacle
Version or Model: FRS-FR
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 00505
Company Name: Healthcraft Products Inc.

Primary DI Number: 00689281005050
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 252468293 *Terms of Use

Device Description: The SuperPole FRS is a high quality, commercial grade support receptacle that is permanently embedded into a structural concrete floor to be used exclusively with the SuperPole FRS-Pole. The SuperPole F.R.S. is intended for moderate vertical load bearing to provide sitting and standing support for people with reduced mobility. When the pole is removed, the receptacle must be covered with a floor flush cap to provide a water-tight seal. The maximum user weight for this product is 450lbs / 205kgs. Product is not intended to support full body weight. The SuperPole F.R.S. is not to be used in any other way than described

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):	No
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?
43235	Fixed-rail armrest	A wall and/or floor fixed-rail system designed to provide arm support for a disabled person to facilitate their movement/mobility. It is permanently-fixed to the wall and/or floor at strategic points in a building or in the home.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
IKX	Aid, Transfer

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: 9cd63544-33d8-49ac-b3e3-4af541f4c0fc
Public Version Date: September 02, 2021
Public Version Number: 1
DI Record Publish Date: August 25, 2021