Identity
- Trade Name
- Power-LOAD FDA UDI
- Generic Name
- Gel-filled bed mattress FDA UDI
- Model / Reference
- 639005550003 FDA UDI
Identifiers
- Catalog Number
- 639005550003 FDA UDI
- Primary DI / UDI-DI
- 07613327504453 FDA UDI
- 510(k) Number
- K113598 FDA UDI
- FDA Product Code
- FPO FDA UDI
- GMDN Term
- Gel-filled bed mattress FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6910 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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Gel-filled bed mattress
Power-LOAD by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Gel-filled bed mattress.
- Drive — Drive Devilbiss Healthcare · Class I
- Gel Foam — Joerns Healthcare · Class I
- Drive — Drive Devilbiss Healthcare · Class I
- Drive — Drive Devilbiss Healthcare · Class I
- Drive — Drive Devilbiss Healthcare · Class I
- Drive — Drive Devilbiss Healthcare · Class I
- Drive — Drive Devilbiss Healthcare · Class I
- DRIVEMEDICAL — Drive Devilbiss Healthcare · Class I
Cleared under the same submission
K113598 also covers:
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 II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Stryker Corp.
Sources (1)
- FDA UDI 257ec58d-2e61-4894-9307-2c7bed8d7ac0 35 fields · synced Jun 8, 2026