Identity
- Trade Name
- CUSHION: TRI-FOAM BARIATRIC 24x20 FDA UDI
- Generic Name
- Wheelchair seat cushion FDA UDI
- Model / Reference
- 11077 FDA UDI
Identifiers
- Catalog Number
- 2970000083 FDA UDI
- Primary DI / UDI-DI
- 00733657216691 FDA UDI
- FDA Product Code
- IMP FDA UDI
- GMDN Term
- Wheelchair seat cushion FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.3920 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
Yes
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
Yes
FDA UDI
Category: Wheelchair seat cushion
CUSHION: TRI-FOAM BARIATRIC 24x20 by AliMed, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Wheelchair seat cushion.
- Spex Limited — SPEX LIMITED · Class I
- Action® — Action Products, Inc. · Class I
- Spex Limited — SPEX LIMITED · Class I
- ROSCOE — COMPASS HEALTH BRANDS CORP. · Class I
- NYOrtho Wheelchair Cushion Gel-Foam 22x20x4 — N.Y. ORTHOPEDIC USA, INC. · Class I
- Spex Limited — SPEX LIMITED · Class I
- Spex Limited — SPEX LIMITED · Class I
- Spex Limited — SPEX LIMITED · 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
- AliMed, LLC
Sources (1)
- FDA UDI f60e2c83-48e7-4deb-95e5-f095136a3f24 34 fields · synced Jun 9, 2026