e2 Ceiling Mount Trapeze with 32 in. Grab Bar (UDI STP-CM-32)
Manufactured by Healthcraft Products Inc.
Device Regulatory Overview
The e2 Ceiling Mount Trapeze with 32 in. Grab Bar (Model/Catalog Number: STP-CM-32) 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
- STP-CM-32
- Product Code / EMDN
- FMR
- Device Name
- The e2 Ceiling Mount Trapeze is an over-bed trapeze system that secures to the ceiling. The trapeze handle features two offset ladder rungs to allow for improved use of arm strength and increased comfort. Additionally, it can slide sideward / laterally on the ceiling mounted grab bar to store out of the way when not in use. The e2 Ceiling Mount Trapeze is intended for moderate vertical load bearing to provide sitting and standing support for people with reduced mobility. The grab bar is installed to a structural ceiling, and a metal hook is looped onto the grab bar. The trapeze handle is connected with an adjustable strap to the metal hook. The maximum user weight for this product is 300lbs / 136kgs. No more than 150lbs / 68kgs is to be exerted on the e2 trapeze (sitting support only). NOTE: Product is not intended to support full body weight.
- 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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of e2 Ceiling Mount Trapeze with 32 in. Grab Bar?
The registered manufacturer of record for e2 Ceiling Mount Trapeze with 32 in. Grab Bar is Healthcraft Products Inc..
What is the Primary UDI-DI identifier for e2 Ceiling Mount Trapeze with 32 in. Grab Bar?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is STP-CM-32.
What classification code is assigned to this device?
This device is registered under product classification code FMR.
Similar Classification Devices (FMR)
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