Identity
- Trade Name
- DynaRest Gel Foam Mattress Overlay FDA UDI
- Generic Name
- Gel-filled bed mattress overlay FDA UDI
- Device Name
- 42" x 76" x 3.5" FDA UDI
- Model / Reference
- 10438 FDA UDI
- Description
- 42" x 76" x 3.5" FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00840117335790 FDA UDI
- FDA Product Code
- FMW FDA UDI
- GMDN Term
- Gel-filled bed mattress overlay FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6190 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
Yes
FDA UDI
Category: Gel-filled bed mattress overlay
DynaRest Gel Foam Mattress Overlay by Dynarex Corp. — 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
- Dynarex Corp.
Sources (1)
- FDA UDI c69ac138-0a92-408e-a1ec-16faa67732ab 33 fields · synced May 30, 2026