ProCuity™ Bed Series Operations Manual 3009 EN 3009-009-001 Rev A.
Symbols Refer to instruction manual/booklet Consult instructions for use General warning Caution Warning; electricity Fuse rating Non-ionizing radiation Catalogue number Serial number European medical device CE mark Authorized representative in the European Community For US Patents see www.stryker.com/patents Manufacturer Safe working load Mass of equipment NAWI Class IIII Maximum patient weight 3009-009-001 Rev A.
Adult patient ~ Alternating current Direct current ≤2m ≥18m Duty cycle of product Unit provides terminal for connection of a potential equalization conductor. The potential equalization conductor provides direct connection between the unit and potential equalization busbar of the electrical installation. Protective earth ground IPX4 Protection from liquid splash Type B applied part 87VL Medical Equipment Classified by Underwriters Laboratories Inc.
Table of Contents Warning/Caution/Note Definition ..............................................................................................................................3 Summary of safety precautions ................................................................................................................................3 Introduction ...............................................................................................................................................................
Raising or lowering the IV pole (option)...................................................................................................................33 Attaching or removing the patient helper (option) .....................................................................................................34 Adjusting the patient helper (option) .......................................................................................................................35 Attaching the oxygen bottle holder......
Warning/Caution/Note Definition The words W A R N I N G , C A U T I O N , and N O T E carry special meanings and should be carefully reviewed. WARNING Alerts the reader about a situation which, if not avoided, could result in death or serious injury. It may also describe potential serious adverse reactions and safety hazards.
• Always unplug the power cord before you transport the product. • Always release the brakes before you transport the product. Do not transport the product with the brakes applied. • Do not transport the product laterally after you apply the steer lock pedal. The product cannot swivel when you transport with steer lock. • Do not attempt to release steer lock while the product is in motion. • Do not use the headboard for CPR support. • Always set the siderail position for appropriate patient safety.
• • • • • Do not load an individual IV pole hook above the safe working load of 20 lb (9 kg). Always secure the lifting pole in the mounting bracket before you adjust the patient helper. Always make sure that the patient helper mounting bracket is secure before use. Do not load the oxygen bottle holder above the safe working load of TBD lb. Always unplug the power cord from the wall outlet when large spills occur near the circuit boards, cables, and motors.
Introduction This manual assists you with the operation or maintenance of your Stryker product. Read this manual before operating or maintaining this product. Set methods and procedures to educate and train your staff on the safe operation or maintenance of this product. CAUTION • Improper usage of the product can cause injury to the patient or operator. Operate the product only as described in this manual. • Do not modify the product or any components of the product.
• Behavioral health patient use • Newborn (neonate) or infant patient use • Oxygen rich environments • Home care or long-term care facility settings Expected service life The P r o C u i t y bed series has a 10 year expected service life under normal use conditions and with appropriate periodic maintenance. The backup batteries have a one year expected service life under normal use conditions.
Bed height to top of seat litter With bed extender accessory 94.5 in. x 35 in. 240 cm x 88.9 cm Standard 12 in. to 30 in. 30.5 cm x 76.2 cm Zoom 14 in. to 32 in. 35.6 cm x 81.3 cm Gatch position 0° to 30° ± 5° Fowler position 0° to 65° ± 5° Trendelenburg and reverse Trendelenburg +12° to -12° ± 5° Electrical requirements N o t e - Class I Electrical Equipment: Protection against electrical shock relies on connection to protective earth of an appropriately rated hospital grade outlet.
Operation Environmental conditions Ambient temperature 50 °F (10 °C) Storage and transportation 95 °F (35 °C) -40 °F (-40 °C) 75% Relative humidity (non-condensing) 95% 30% 10% 106 kPa Atmospheric pressure 140 °F (60 °C) 70 kPa 106 kPa 50 kPa Wi-Fi radio specifications (option) Manufacturer/model Silex SX-SDMAC-2832S+ Chipset Qualcomm QCA9377-3 IEEE 802.11 a/b/g/n/ac RF bands 2.
Specification - Chipset QCA9377-3 (Qualcomm Atheros) Item Unit Band 5GHz Max 11g/n/ac 2422 2462 MHz 11a/n/ac 5180 5825 MHz 11n/ac 5190 5795 MHz 11ac 5210 5775 MHz 5 MHz 11a/n/ac 20 MHz 11n/ac 40 MHz 11ac 80 MHz Not applicable 11b DSSS (DBPSK, DQPSK, CCK) Not applicable Not applicable 11a/g/n OFDM (BPSK, QPSK, 16QAM, 64QAM) Not applicable Not applicable 11ac OFDM (BPSK, QPSK, 16QAM, 64QAM, 255QAM) Not applicable Not applicable Not applicable -8.
Customer network communication requirements for iBed Wireless (option) LAN environment Wi-Fi radio communication Note IPv4 only Static Wi-Fi radio IP allocation DHCP Not applicable • If Static - Unique IP address will be required for each Wi-Fi radio MAC address • If DHCP and not using a DNS name - Each Wi-Fi radio MAC address will need a reserved IP address • If DHCP and using a DNS name - It is required to create a unique name for each Wi-Fi radio MAC address for Wi-Fi radio management ∘ Stryker
Required Customer WLAN environment Max number of SSIDs 5 Recommended Authentication timeouts Add session timeout of at least 24 hours Recommended N o t e - A transmit power asymmetry problem may arise at the edges of virtual cell coverage if an AP’s transmit power is higher than the Wi-Fi radio (~6 mW 2.4 GHz or 12 mW 5 GHz). Verify the received signal strength indicator (RSSI) of the Wi-Fi radio on the AP. The Wi-Fi radio should never drop below an RSSI of -75 dBm on the AP.
Applied parts Figure 2 – Type B applied parts Contact information Contact Stryker Customer Service or Technical Support at: 1-800-327-0770. Stryker Medical 3800 E. Centre Avenue Portage, MI 49002 USA N o t e - The user and/or the patient should report any serious product-related incident to both the manufacturer and the Competent authority of the European Member State where the user and/or patient is established. To view your operations or maintenance manual online, see https://techweb.stryker.com/.
Setup W A R N I N G - Always plug the product into a grounded, hospital grade wall outlet. You can only achieve grounding reliability when you use a hospital grade wall outlet. This product is equipped with a hospital-grade plug for protection against electric shock hazard. C A U T I O N - Do not clean, disinfect, service, or perform maintenance while the product is in use. N o t e - Allow the product to reach room temperature before you conduct any setup or test functional operations.
To setup nurse call communication: N o t e - The product is equipped with an input that accepts a DB-37 nurse call cable. 1. Plug the interface cable into the 37-pin connector on the litter frame at the head end of the product (A) (Figure 3). N o t e - Only connect the 37-pin connector to the 37-pin connection on the product or the product Communications Tester (sold separately). 2. Plug the interface cable into the applicable connection (patient station, head wall, or docker station). 3.
Operation Plugging or unplugging the product WARNING • Always connect this product to a supply mains with protective earth to avoid the risk of electric shock. • Always make sure the product is connected to an appropriate power source if the loss of power would result in unacceptable risk. • Always allow enough clearance between the head end of the product and the adjacent wall, so you can unplug the power cord from the wall outlet. • Always store the power cord before you transport the product.
Storing the power cord WARNING • Always store the power cord before you transport the product. • Always store the power cord to avoid the risk of entanglement, damage to the power cord, or potential shock hazards. If the power cord is damaged, remove the product from service. C A U T I O N - Do not pinch the power cord in the bed frame. To store the power cord and auxiliary cord, wrap the cords and secure them with the cord wrap (A) under the head end of the product (Figure 4).
Applying or releasing the brakes WARNING • Always apply the brakes when a patient is getting into or out of the product to avoid instability. • Always apply the brakes when the patient is unattended. • Do not apply the brakes to slow or stop the product while the product is in motion. You can find the brake pedals at the head end and foot end of the product. To apply the brakes, depress the red side of the pedal (Figure 5). The brake pedal locks all four casters to hold the product in place.
Figure 7 – Applying steer lock Figure 8 – Releasing steer lock/neutral position Activating the CPR release handle C A U T I O N - Always make sure that all persons and equipment are away from the area below and around the Fowler before you activate the CPR release handle. The CPR release handle is for emergency use only. When you raise the Fowler and need quick access to the patient, pull the CPR release handle to position the product to 0°.
Removing or replacing the footboard You can remove the footboard (G) (Product illustration (page 12)) to access the patient or to clean the product. To remove the footboard: 1. Grasp the handles and lift the footboard straight up and off the product. To replace the footboard: 1. Align the footboard pegs with the sockets at the foot end of the product. 2. Lower the footboard until the footboard seats into the sockets.
Figure 12 – Siderail lowest position Securing a Foley bag to the Foley bag hook Note • The safe working load of the Foley bag hook is 10 lb (4.5 kg). • Do not allow the Foley bag to touch the ground while the product is in low height. There are two Foley bag hooks under the foot section (L) (Product illustration (page 12)), one on either side of the product. To secure a Foley bag, place the hook of the Foley bag on the Foley bag hook.
A Bed exit Press and hold to cancel bed exit alarm B Nurse call Activates nurse call C Gatch up Raises the Gatch D Gatch down Lowers the Gatch E Fowler up Raises the Fowler F Fowler down Lowers the Fowler G Fowler 30°+ Illuminates when the Fowler is 30°+ H Bed height up Raises the litter I Bed height down Lowers the litter J Brake indicator Illuminates when you apply or release the brake Operator control panel, advanced, outside siderail (option) WARNING • Always lower the prod
C Patient ingress/egress Places the product into a position for patient ingress or egress N o t e - The patient ingress or egress button disables bed exit.
D Gatch up Raises the Gatch E Gatch down Lowers the Gatch Pendant, basic (option) TBD Healthcare professionals must instruct patients how to operate the pendant. Pendant, advanced (option) TBD Healthcare professionals must instruct patients how to operate the pendant. Footboard control panel - Menu controls The menu controls are located on the touch panel of the footboard. Press the icons to display the functions of the product.
G Settings Displays settings (Footboard control panel - Settings (page 31)) H Brake Basic - Displays brake lock status Advanced (option) - Apply or release the brakes (Applying or releasing the brakes (page 18)) Footboard control panel - Position WARNING • Always lower the product to its lowest height when the patient is unattended to reduce the risk of injury due to patient falls.
M Vascular position Places the product into the vascular position N Back Returns to the P o s i t i o n screen Footboard control panel - Motion Lock WARNING • Always lock the controls when the patient is unattended. • Always lock the controls when the patient's condition requires extra safety measures. The M o t i o n L o c k screen displays the lockout functions of the product. Lockouts can lock out motion control input from the operator control panel and patient control panel.
A Home Returns to the H o m e screen (Footboard control panel Menu controls (page 24)) B Info Displays the S c a l e I n f o screen C Save Weight Select to save the current displayed weight (Weighing a patient (page 28)) D Zero (Non-NAWI) Tare (NAWI) Select to zero/tare the scale or set the scale for a new patient (Zeroing/taring the scale (page 27)) E Add Equip.
Weighing a patient WARNING • Do not use the scale system reading as a reference for medical treatment. • The scale system assists only to monitor the patient’s weight variation. Before you place a patient on the product, make sure that you zero/tare the scale (Zeroing/taring the scale (page 27)). N o t e - Always zero/tare the scale after you add a support surface, mattress, or linens to the product. To weigh a patient: 1.
To add or remove equipment: 1. Press the S c a l e button (D) on the footboard control panel (Footboard control panel - Menu controls (page 24)). 2. On the S c a l e screen, press the A d d E q u i p . button (E) (Footboard control panel - Scale (page 26)). 3. One item at a time, add or remove the desired equipment from the product. N o t e - Do not touch the product while the product weighs the equipment. 4. Press the S a v e button to save the current weight and equipment count.
N o t e - If you do not set the scale to zero before you place a patient on the product, bed exit may not operate as intended. 2. Position the patient on the product. 3. Press the B e d E x i t button (B) on the footboard control panel to arm bed exit (Footboard control panel - Menu controls (page 24)). 4. Select the desired zone (B, C, D) (Footboard control panel - Bed exit (page 29)).
I Bed Flat Monitor the bed flat position J Turn Off Turn off i B e d Watch K Exit Returns to the i B e d W a t c h O n screen Enabling or disabling iBed Watch To enable i B e d Watch: 1. Position the patient on the product. 2. Press the i B e d W a t c h button (C) on the footboard control panel to enable i B e d Watch (Footboard control panel - Menu controls (page 24)). 3. Select the desired bed settings to monitor (Footboard control panel - i B e d Watch (page 30)).
Settings F Displays settings Displays advanced settings G Advanced N o t e - Press and hold the S e t t i n g s button (F) to display the advanced settings button.
Accessories and parts These accessories and parts may be available for use with your product. Confirm availability for your configuration or region.
A C B Figure 13 – Two-stage IV pole Attaching or removing the patient helper (option) W A R N I N G - Always use two people to attach or remove the patient helper. CAUTION • Always secure the lifting pole in the mounting bracket before you adjust the patient helper. • Always remove the patient helper before you transport the product. You can attach the patient helper into the patient helper mounting bracket at the head end of the product. To attach the patient helper: 1.
A C B Figure 14 – Attaching or removing the patient helper Reverse steps to remove the patient helper. Adjusting the patient helper (option) W A R N I N G - Do not load the patient helper above the safe working load of 200 lb (90.7 kg). CAUTION • Always secure the lifting pole in the mounting bracket before you adjust the patient helper. • Do not use the patient helper as a push or pull device. • Always make sure that the patient helper mounting bracket is secure before use.
C B A Figure 15 – Adjusting the patient helper Attaching the oxygen bottle holder CAUTION • Do not load the oxygen bottle holder above the safe working load of TBD lb. • Do not use the oxygen bottle holder as a push or pull device. To attach the oxygen bottle holder: 1. Insert the oxygen bottle holder support bar into the accessory socket that is located on either side of the product at the head end and foot end. EN 36 3009-009-001 Rev A.
Cleaning and disinfecting with wipes For United States only. Confirm availability for your configuration or region. Call Stryker Customer Service: 1-800-3270770. Stryker’s preferred wipes (2060-000-001 6'' x 10'' or 2060-000-002 9'' x 12'') include the following active ingredients: • n-Alkyl (60% C14, 30% C16, 5% C12, 5% C18) dimethyl benzyl ammonium chloride - 0.154% • n-Alkyl (68% C12, 32% C14) dimethyl ethylbenzyl ammonium chloride - 0.154% • Isopropanol - 21.
Cleaning CAUTION • Do not clean, disinfect, service, or perform maintenance while the product is in use. • Always unplug the power cord from the wall outlet when large spills occur near the circuit boards, cables, and motors. Remove the occupant from the product, clean up the fluid, and inspect the product. Fluids can cause unpredictable operation and decreased functionality of any electrical product. Do not return the product to service until dry and tested for safe operation.
Disinfecting CAUTION • Do not clean, disinfect, service, or perform maintenance while the product is in use. • Always unplug the power cord from the wall outlet when large spills occur near the circuit boards, cables, and motors. Remove the occupant from the product, clean up the fluid, and inspect the product. Fluids can cause unpredictable operation and decreased functionality of any electrical product. Do not return the product to service until dry and tested for safe operation.
Preventive maintenance Remove the product from service before you perform the preventive maintenance inspection. Check all items listed during annual preventive maintenance for all Stryker Medical products. You may need to perform preventive maintenance checks more often based on your level of product usage. Service only by qualified personnel. N o t e - Clean and disinfect the exterior of the support surface before inspection, if applicable.
Wireless notifications For product equipped with optional wireless communication technology, these statements apply to the countries as indicated: Country Notification Contains IC ID: 4919E-SDMACP Contains IC ID: 5123A-BGTWT32I Canada This device complies with Innovation, Science and Economic Development Canada’s licenseexempt RSSs.
EMC information WARNING • Portable RF communications equipment, including peripherals such as antenna cables and external antennas, should be no closer than 12 inches (30 cm) to any part of P r o C u i t y bed series, including cables specified by the manufacturer. • Avoid stacking or placing equipment adjacent with other equipment to prevent improper operation of the product. If such use is necessary, carefully observe stacked or adjacent equipment to make sure that they operate properly.
Guidance and manufacturer’s declaration - electromagnetic immunity Electrostatic fast transient/ burst IEC 61000-4-4 ±2 kV for power supply lines ±1 kV for input/output lines ±2 kV for power supply lines ±1 kV for input/output lines Main power quality should be that of a typical commercial or hospital environment. Surge IEC 61000-4-5 ±0.5 kV, ±1 kV lines to lines ±0.5 kV, ±1 kV, ±2 kV lines to earth ±0.5 kV, ±1 kV lines to lines ±0.
Portable and mobile RF communications equipment should follow the guidance in the table titled “Recommended separation distances between portable and mobile RF communication equipment and the 3009 P r o C u i t y bed series.” If the mobile service is not listed in the table, the recommended separation distance should be calculated from the equation appropriate for the frequency of the transmitter. Conducted RF IEC 61000- 4-6 Radiated RF IEC 61000-4-3 3 Vrms 150 kHz to 80 MHz 3 V/m 80 MHz to 2.
Recommended separation distances between portable and mobile RF communication equipment and the 3009 ProCuity bed series The 3009 P r o C u i t y bed series is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled.
Stryker Medical 3800 E. Centre Avenue Portage, MI 49002 USA 3009-009-001 Rev A.0 WCR: AA.
