DINAMAP PRO Series 100-400V2 Monitor - GTS …

1 1 DINAMAP PROS eries 100-400V2 MonitorOperation Manual2 DINAMAP PRO 400v2 Monitor3 DINAMAP PRO MonitorOperation ManualThis manual is for DINAMAP PRO Monitor Models 100V2, 200V2, 300V2, and 400v2 , all with printers. PRO 100V2: BP and Pulse PRO 200V2: BP, Pulse, and Temp PRO 300V2: BP, Pulse, and SpO2 PRO 400v2 : BP, Pulse, Temp, and SpO2 The model of the Monitor determines which menu option buttons appear on the LCD. Please refer to applicable sections. The Model Number 100-400V2 is generic in nature and reflects the range of product codes available. Your product may be labeled with a specific product code such as DINAMAP PRO Model 410. "V2" refers to the second version of the product's design.

2 Reissues and UpdatesChanges occurring between issues are addressed through Change Information Sheets, Addendums, and replacement pages. If a Change Information Sheet does not accompany this manual, it is correct as and OmissionsIf errors or omissions are found in this manual, please notify:GE Medical Systems Information Technologies4502 Woodland Corporate BoulevardTampa, FL 336141-877-274-8456 Part No. 2009802-001 BThe content of this document including all figures and drawings is proprietary information of GE Medical Systems Information Technologies, provided solely for purposes of operation, maintenance or repair, and dissemination for 4other purposes or copying thereof is prohibited without prior written consent by GE Medical Systems Information Technologies, Tampa, may show design models; production units may incorporate of Warnings and CautionsA general warning is a statement that alerts the user to the possibility of injury, death, or other serious adverse reactions associated with the misuse of the device.

3 A warning relates to steps in a general caution is a statement that alerts the user to the possibility of a problem with the device associated with its use or misuse. Such problems include device malfunction, device failure, damage to the device or damage to other property. A caution relates to steps in a procedure. GE Medical Systems Information Technologies, 2002. All rights reserved. Tampa, FL 33614 Printed in the United StatesGE Medical Systems Information Technologies4502 Woodland Corporate BoulevardTampa, FL 33614 European RepresentativeGE Medical Systems Information Technologies GmbHPostfach 60 02 65D-79032 Freiburg, GermanyTel. +49 761 45 43 - 0 Fax +49 761 45 43 - 2335 Introduction.

4 7 About the DINAMAP PRO Monitor .. 7 Product Compliance ..10 Symbols ..11 Getting 13 Unpacking the Monitor and Accessories ..13 Power Sources ..13 Powering the Monitor ..13 Rear Panel Connections ..16 Front Panel Controls and Indicators ..17 Switching the Monitor On and Crystal Display (LCD)..19 Using the Printer ..20 Installing the Paper ..20 Printer Alarms ..21 Storage ..22 Using the Monitor .. 23 Noninvasive Blood Pressure Determination .. Mode ..29 Auto Mode ..29 Stat Mode ..30 TURBO* SET SpO2 ..37 NELLCOR OxiMAXTM the Menu System .. Crystal ..58 Menu Tree ..58 Main Button (UK: All Obs) .. BP Button (UK: BP Mode)..60 Alarms Button ..62 Trend Button.

5 63 Print Button .. Menu ..66 SpO2 Button ..66 Config Sav (Sleep Mode) ..68 Time ..69 Rotor .. Button ..70 Service Menu ..72 Error and Warning Messages ..75 Alarms Button ..75OK 77 Technical ..82 Power Requirements ..82 Environmental ..83 Appendix B .. 85 Patient Alarms ..85 Failsafe of 91 Principles of Noninvasive Blood Pressure D .. 95 Reorder E .. 97 Warranty, Service, and Spare Parts .. Manuals ..98 Appendix F .. 99 Maintenance ..99 Cleaning the Monitor ..99 Cuff Cleaning and Disinfection ..99 Temperature Devices .. 100 SpO2 100 Storage and Battery Care .. 101 Fuses .. 102 Calibration .. 102 Leak 102 Disposal of Product Waste .. 103 Appendix G.

6 105 Host Port Connector (rear panel).. 1057 About the DINAMAP PRO MonitorDINAMAP PRO Monitors provide noninvasive determination of systolic blood pressure, diastolic blood pressure, mean arterial pressure, pulse rate, temperature, and oxygen saturation. These portable AC- and DC-operated monitors are primarily intended for use in hospital acute care settings such as outpatient surgery, accident and emergency, labor and delivery, GI/endoscopy, and medical/surgical PRO Monitor comes in four different models: PRO 100V2, 200V2, 300V2, and 400v2 , all with printers. PRO 100V2: BP and Pulse PRO 200V2: BP, Pulse, and Temp PRO 300V2: BP, Pulse, and SpO2 PRO 400v2 : BP, Pulse, Temp, and SpO2 All of the main operations of the PRO Monitor are easy to use.

7 Please review the factory default settings and, where applicable, enter settings appropriate for your use. The Using the Monitor section of this manual explains how to use the Monitor in its most simple form, while the Using the Menu System section explains how to customize measurements by using the menu PRO Monitor is intended to Monitor one patient at the bedside. ContraindicationsThis device is not designed, sold, or intended for use except as law ( ) restricts this device to sale by or on the order of a Do not use the PRO Monitor in the presence of magnetic resonance imaging (MRI) devices. There have Introduction8been reports of sensors causing patient burns when operating in an MRI environment.

8 Do not use the Monitor in the presence of flammable anesthetics. To help prevent unintended current return paths with the use of high frequency (HF) surgical equipment, ensure that the HF surgical neutral electrode is properly connected. To avoid personal injury, do not perform any servicing unless qualified to do so. WARNING: These Monitors should not be used on patients who are connected to cardiopulmonary bypass machines. If powering the Monitor from an external power adapter or converter, use only power adapters and converters approved by GE Medical Systems Information Technologies. The Monitor does not include any user-replaceable fuses. Refer servicing to qualified service personnel.

9 To reduce the risk of electric shock, do not remove the cover or the back. Refer servicing to a qualified service person. If the accuracy of any determination reading is questionable, first check the patient s vital signs by alternate means and then check the PRO Monitor for proper Do not use replacement batteries other than the type supplied with the Monitor . Replacement batteries are available from GE Medical Systems Information Technologies. See Appendix D. The PRO Monitor is designed to conform to Electromagnetic Compatibility (EMC) standard IEC 601-1-2, 1993 and will operate accurately in conjunction with other medical equipment which also meets this requirement. To avoid interference problems affecting the Monitor , do not use the Monitor in the 9presence of equipment which does not conform to these specifications.

10 Place the PRO Monitor on a rigid, secure surface. Monitor must only be used with mounting hardware, poles, and stands recommended by GE Medical Systems Information Technologies. See Appendix D. The weight of the accessory basket contents should not exceed lb (3 kg). Arrange the power cord, air hoses, and all cables carefully so they do not constitute a hazard. Verify calibration of BP parameter (temp and pulse oximeter do not require calibration). Ensure that the display is functioning properly before operating the PRO Monitor . Do not immerse the Monitor in water. If the Monitor is splashed with water or becomes wet, wipe it immediately with a dry cloth. Do not gas sterilize or autoclave.