e2™ Trapeze Handle & Strap

FDA UDI

Class I (US FDA UDI)

by Healthcraft Products Inc.

Identity

Trade Name: e2™ Trapeze Handle & Strap FDA UDI
Generic Name: Hand rail FDA UDI
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. The e2 Ceiling Mount Trapeze is not to be used in any other way than described. FDA UDI
Model / Reference: STP-HS FDA UDI
Description: 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. The e2 Ceiling Mount Trapeze is not to be used in any other way than described. FDA UDI

Identifiers

Catalog Number: 02042 FDA UDI
Primary DI / UDI-DI: 00689281020428 FDA UDI
FDA Product Code: IKX FDA UDI
GMDN Term: Hand rail FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 890.5050 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Hand rail

e2™ Trapeze Handle & Strap by Healthcraft Products Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hand rail.

Drive — Drive Devilbiss Healthcare · Class I
Drive — Drive Devilbiss Healthcare · Class I
Drive — Drive Devilbiss Healthcare · Class I
Quick release adapter(A) — Shenzhen Mindray Bio-Medical Electronics Co. · Class II
Rolling stand(BeneVision N19/N22) — Shenzhen Mindray Bio-Medical Electronics Co. · Class II
Drive — Drive Devilbiss Healthcare · Class I
Drive — Drive Devilbiss Healthcare · Class I
VIVE — VIVE HEALTH LLC · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Healthcraft Products Inc.

Sources (1)

FDA UDI 070f7f0a-235e-45ee-8f68-8d4006be241e 34 fields · synced May 29, 2026