GUDIDData
gudid Primary ID: SP-PU

Packing, SuperPole Ultra Pole in Shipping Tube, SPHDU (UDI SP-PU)

Manufactured by Healthcraft Products Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Packing, SuperPole Ultra Pole in Shipping Tube, SPHDU - Primary ID SP-PU

Device Regulatory Overview

The Packing, SuperPole Ultra Pole in Shipping Tube, SPHDU (Model/Catalog Number: SP-PU) 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-PU
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 Ceiling height 121-140" / 3073-3556mm Max User Weight 300lbs / 136kg
Database Sync Date
2026-08-09 09:04:23

Full Regulatory Attributes

🔒 Token Gated
{
    "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 Packing, SuperPole Ultra Pole in Shipping Tube, SPHDU?

The registered manufacturer of record for Packing, SuperPole Ultra Pole in Shipping Tube, SPHDU is Healthcraft Products Inc..

What is the Primary UDI-DI identifier for Packing, SuperPole Ultra Pole in Shipping Tube, SPHDU?

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

What classification code is assigned to this device?

This device is registered under product classification code FMR.

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