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Parts Box, SuperPole Ultra, SPHDU

FDA UDI

Class I (US FDA UDI)

by Healthcraft Products Inc.

Identity

Trade Name
Parts Box, SuperPole Ultra, SPHDU FDA UDI
Generic Name
Hand rail FDA UDI
Device Name
The SuperPole Ultra is a high quality, commercial grade floor to ceiling safety pole (intended usage same as SuperPole). The SuperPole Ultra is intended for applications with floor to ceiling ranges from 121-140" / 3073-3556mm. The SuperPole Ultra is not to be used with the SuperBar, SuperTrapeze, Angled Ceiling Plate or Uni-Fit Extender. The SuperPole Ultra parts (pole, extension tube and top plate - labelled for convenience) should not be used with the components of any other floor to ceiling poles. FDA UDI
Model / Reference
SP-BXU FDA UDI
Description
The SuperPole Ultra is a high quality, commercial grade floor to ceiling safety pole (intended usage same as SuperPole). The SuperPole Ultra is intended for applications with floor to ceiling ranges from 121-140" / 3073-3556mm. The SuperPole Ultra is not to be used with the SuperBar, SuperTrapeze, Angled Ceiling Plate or Uni-Fit Extender. The SuperPole Ultra parts (pole, extension tube and top plate - labelled for convenience) should not be used with the components of any other floor to ceiling poles. FDA UDI

Identifiers

Catalog Number
01557 FDA UDI
Primary DI / UDI-DI
00689281015578 FDA UDI
FDA Product Code
FMR FDA UDI
GMDN Term
Hand rail FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6785 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Hand rail

Parts Box, SuperPole Ultra, SPHDU by Healthcraft Products Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hand rail.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 274beb6e-f7fc-4d70-bc48-bbb239c22b1f 34 fields · synced May 31, 2026