Parts Box, SuperPole Heavy Duty - The SuperPole is a high quality, commercial grade - Healthcraft Products Inc.

Duns Number:252468293

Device Description: The SuperPole is a high quality, commercial grade floor to ceiling safety pole. The SuperP The SuperPole is a high quality, commercial grade floor to ceiling safety pole. The SuperPole is intended for moderate vertical and horizontal load bearing to provide sitting and standing support for people with reduced mobility. The SuperPole is installed between a structural floor and ceiling by turning a jackscrew at the bottom of the pole. The pressure created by the jackscrew is strong enough for the SuperPole to support the user, yet it does not require drilling holes into the floor or ceiling. This is ideal for relocating or removing the pole. The floor to ceiling range and maximum user weight dependent on model. Note: Product is not intended to support full body weight.The SuperPole is not to be used in any other way than described above. The SuperPole is made from robust materials and is capable of supporting vigorous forces during proper / normal usage. The structural components of the pole are made from metal. The components of the pole that make direct contact with the floor and ceiling are made of non-slip rubber to protect the surfaces from damage, as well as provide traction. The top plate and base plate can be easily separated from the pole by use of multiple use fasteners (clevis and cotter pin). The top plate can be secured to the structural ceiling joist with wood screws: - if regular inspection (and if necessary, tightening) cannot be done - if pole is subjected to aggressive usage - if using SuperPole Heavy Duty (SP-HD)

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More Product Details

Catalog Number

01540

Brand Name

Parts Box, SuperPole Heavy Duty

Version/Model Number

SP-BXHD

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

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)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

-

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code Details

Product Code

FMR

Product Code Name

Device, Transfer, Patient, Manual

Device Record Status

Public Device Record Key

17c04062-92ae-40a9-98e8-484880b6f9a8

Public Version Date

September 02, 2021

Public Version Number

1

DI Record Publish Date

August 25, 2021

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"HEALTHCRAFT PRODUCTS INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 298