Identity
- Trade Name
- SuperTrapeze™ Add On Kit FDA UDI
- Generic Name
- Hand rail FDA UDI
- Device Name
- The SuperTrapeze is a high quality, commercial grade over-bed trapeze that connects to the SuperPole (floor to ceiling safety pole). The SuperTrapeze handle features two offset ladder rungs to allow for improved use of arm strength and increased comfort. Additionally, it can hook around the pole to store out of the way when not in use. The support arm has an adjustable strap that attaches to the trapeze handle. It is important to set proper height and orientation of the SuperTrapeze to optimize the user’s range of motion. FDA UDI
- Model / Reference
- STP-AK FDA UDI
- Description
- The SuperTrapeze is a high quality, commercial grade over-bed trapeze that connects to the SuperPole (floor to ceiling safety pole). The SuperTrapeze handle features two offset ladder rungs to allow for improved use of arm strength and increased comfort. Additionally, it can hook around the pole to store out of the way when not in use. The support arm has an adjustable strap that attaches to the trapeze handle. It is important to set proper height and orientation of the SuperTrapeze to optimize the user’s range of motion. FDA UDI
Identifiers
- Catalog Number
- 02011 FDA UDI
- Primary DI / UDI-DI
- 00689281020114 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
SuperTrapeze™ Add On Kit by Healthcraft Products Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 |
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Manufacturer
- Manufacturer
- Healthcraft Products Inc.
Sources (1)
- FDA UDI cbeb84a1-db95-431b-b388-713cc9fdd368 34 fields · synced May 30, 2026