GUDIDData
gudid Primary ID: SP-ACP-BX

Parts Box, SuperPole Angled Ceiling Plate (UDI SP-ACP-BX)

Manufactured by Healthcraft Products Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Parts Box, SuperPole Angled Ceiling Plate - Primary ID SP-ACP-BX

Device Regulatory Overview

The Parts Box, SuperPole Angled Ceiling Plate (Model/Catalog Number: SP-ACP-BX) 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-ACP-BX
Product Code / EMDN
FMR
Device Name
The Angled Ceiling Plate (ACP) is a high quality, commercial grade installation accessory to be used with the SuperPole. The ACP is intended to permit the SuperPole to be installed in areas where the ceiling is vaulted or angled. The ACP attaches to the top of the pole and is adjustable in angle from 0-45. The ACP must be secured to ceiling joists with appropriate fasteners. The ACP is only to be used with HealthCrafts SuperPole System. The ACP is not to be used with the SuperPole Bariatric, SuperPole Ultra and Ceiling Plate Extender. The ACP is not to be used in any other way than described above.
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 Parts Box, SuperPole Angled Ceiling Plate?

The registered manufacturer of record for Parts Box, SuperPole Angled Ceiling Plate is Healthcraft Products Inc..

What is the Primary UDI-DI identifier for Parts Box, SuperPole Angled Ceiling Plate?

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

What classification code is assigned to this device?

This device is registered under product classification code FMR.

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