Identity
- Trade Name
- Action® FDA UDI
- Generic Name
- Gel-filled bed mattress overlay FDA UDI
- Device Name
- Mattress Overlay FDA UDI
- Model / Reference
- Mattress Overlay FDA UDI
- Description
- Mattress Overlay FDA UDI
Identifiers
- Catalog Number
- 6300 FDA UDI
- Primary DI / UDI-DI
- 00089904002204 FDA UDI
- FDA Product Code
- IKY FDA UDI
- GMDN Term
- Gel-filled bed mattress overlay FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.5150 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: Gel-filled bed mattress overlay
Action® by Action Products, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Action® — Action Products, Inc. · Class I
- Action® — Action Products, Inc. · Class I
- Action® — Action Products, Inc. · Class I
- Action® — Action Products, Inc. · 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 |
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Manufacturer
- Manufacturer
- Action Products, Inc.
Sources (1)
- FDA UDI 7e3759b9-858c-4388-9a13-6c26538893c9 36 fields · synced Jun 9, 2026