gudid Primary ID: SP-S

SuperPole (UDI SP-S)

Manufactured by Healthcraft Products Inc.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The SuperPole (Model/Catalog Number: SP-S) is a medical device manufactured by Healthcraft Products Inc.. This product is indexed under FDA Product Code / Category Classification FMR within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: SP-S
Product Code / EMDN: FMR
Device Name: The SuperPole is a high quality, commercial grade floor to ceiling safety pole. The SuperPole must be 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. NOTE: The top plate has two holes that may be used to fix the plate directly to the ceiling joist if necessary. Do not install the pole where it is directly exposed to water. Max user Weight 300lbs / 136kg ceiling height range 03-99" / 2362-2515mm
Database Sync Date: 2026-08-09 09:04:23

Full Regulatory Attributes

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{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of SuperPole?

The registered manufacturer of record for SuperPole is Healthcraft Products Inc..

What is the Primary UDI-DI identifier for SuperPole?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SP-S.

What classification code is assigned to this device?

This device is registered under product classification code FMR.

Similar Classification Devices (FMR)

Other Devices by Healthcraft Products Inc.

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