SkinGuard® Series
Owner’s Manual
PN 400901 Rev. C
ECO 18-0281
Page 9
Support Surface Sanitation:
Complete support surface is made of superior quality materials and is modular in construction. All components
such as manifold, hose assembly, air cushions, top sheet, and base are interchangeable and can be easily
cleaned or detached for laundry.
Disposal Requirements:
This equipment should be disposed of at your local Recycling Center (Non-hazardous waste) when it has
reached the end of its service life.
SAFETY AGENCY APPROVALS
ETL Listed: 3
rd
Edition
The standard for safety of Medical Electrical Equipment
Flame Resistance:
Unit components meet UL 94V-0. Mattress components pass California117.
Optional California TB 106, TB 129, 16 CFR 1632, 16 CFR 1633, BS 6607 (CRIB 5), BS 597-1, & BS-597-2
compliant mattresses lined with Kevlar fire barrier available (Kevlar lining based on flammability standard).
FDA REGISTRATION
FDA registered company as a manufacturer and as a contract manufacturer.
KAP Medical’s quality system meets the requirements of:
FDA 21 CFR, PART 820
– QSR – Current Good Manufacturing Practices (cGMP) for medical devices and ISO
13485.
ISO 13485 certified company.
Medicare coded (SADMERC).
PATENTS
US & International Patents pending.
CERTIFICATE OF ORIGIN
All products are manufactured in Corona, CA, USA.
MADE IN THE USA
