← Back to catalogue

Power-LOAD

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
Power-LOAD FDA UDI
Generic Name
Ambulance stretcher loader FDA UDI
Model / Reference
6390 FDA UDI

Identifiers

Catalog Number
639005550001 FDA UDI
Primary DI / UDI-DI
07613327394740 FDA UDI
510(k) Number
K113598 FDA UDI
FDA Product Code
FPO FDA UDI
GMDN Term
Ambulance stretcher loader 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: Ambulance stretcher loader

Power-LOAD by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ambulance stretcher loader.

Cleared under the same submission

K113598 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI d44a9299-73d1-4894-ae2e-a40607b33699 35 fields · synced May 30, 2026