Identity
- Trade Name
- SLIDING BOARD,8X24,TWO CUTOUTS FDA UDI
- Generic Name
- Wheelchair lap tray FDA UDI
- Model / Reference
- 5086 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00840314801616 FDA UDI
- FDA Product Code
- IMX FDA UDI
- GMDN Term
- Wheelchair lap tray FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.3910 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Wheelchair lap tray
Sliding Board, 8x24, Two Cutouts by Hausmann Enterprises, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Wheelchair lap tray.
- Jenx — JENX LIMITED · Class I
- Jenx — JENX LIMITED · Class I
- Jenx — JENX LIMITED · Class I
- Drive — Drive Devilbiss Healthcare · Class I
- Jenx — JENX LIMITED · Class I
- Drive — Drive Devilbiss Healthcare · Class I
- Top Drop — Therafin Corporation · Class I
- Drive — Drive Devilbiss Healthcare · 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
- Hausmann Enterprises, Llc
Sources (1)
- FDA UDI 4ca6fce3-b024-4ea9-af77-c9339ebdbd86 32 fields · synced Jun 1, 2026