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Switch to Threaded Mode. Show Likes. View Profile. Private Message. Follow User. Forum Posts. The latest letter of the alphabet added to the table below corresponds to the most current revision. B Updated CE marking information. This manual supplies technical information for service representatives and technical personnel so they can maintain the equipment to the assembly level. Use it as a guide for maintenance and electrical repairs considered field repairable.
Where necessary the manual identifies additional sources of relevant information and technical assistance. See the operator's manual for the instructions necessary to operate the equipment safely in accordance with its function and intended use.
A paper copy of this manual will be provided upon request. Contact your local GE representative and request the part number on the first page of the manual. The information presented in this section is important for the safety of both the patient and operator.
This chapter describes how the terms Danger, Warning, Caution, Important, and Note are used throughout the manual. In addition, standard equipment symbols are defined. GE is responsible for the effects on safety, reliability, and performance only if:. This device is intended for use under the direct supervision of a licensed health care practitioner.
This device is not intended for home use. Federal law restricts this device to be sold by or on the order of a physician. Contact GE for information before connecting any devices to the equipment that are not recommended in this manual. Periodically, and whenever the integrity of the device is in doubt, test all functions.
Consideration relating to the choice shall include:. If the installation of the equipment, in the USA, will use V rather than V, the source must be a center-tapped, V, single-phase circuit.
Extreme care has been taken to use fictitious names and related information in the examples and illustrations provided herein. Any similarity of this data to persons either living or dead and to either current or previously existing medical institutions should be regarded as coincidental.
The terms danger, warning, and caution are used throughout this manual to point out hazards and to designate a degree or level or seriousness. Familiarize yourself with their definitions and significance. Hazard is defined as a source of potential injury to a person. WARNING indicates a potential hazard or unsafe practice which, if not avoided, could result in death or serious injury. NOTE provides application tips or other useful information to assure that you get the most from your equipment.
There have been reports of sensors causing patient burns when operating in an MRI environment. The use of approved accessories will provide protection from burns during HF surgery. 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.
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 GE Medical Systems Information Technologies -approved power adapters and converters. The Monitor does not include any user-replaceable fuses. Refer servicing to qualified service personnel. To reduce the risk of electric shock, do not remove the cover or the back. Refer servicing to a qualified service person.
Use of portable phones or other radio frequency RF emitting equipment near the system may cause unexpected or adverse operation. The equipment or system should not be used adjacent to, or stacked with, other equipment.
If adjacent or stacked use is necessary, the equipment or system should be tested to verify normal operation in the configuration in which it is being used. The use of accessories, transducers and cables other than those specified may result in increased emissions or decreased immunity performance of the equipment or system.
Do not use replacement batteries other than the type supplied with the Monitor. The V Monitor is designed to conform to Electromagnetic Compatibility EMC standard IEC 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 presence of equipment which does not conform to these specifications.
Place the V Monitor on a rigid, secure surface. Monitor must only be used with mounting hardware, poles, and stands recommended by GE Medical Systems Information Technologies. Verify calibration of NIBP parameter temperature and pulse oximeter do not require calibration. Ensure that the display is functioning properly before operating the V 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.
The V Monitor, when used with GE Medical Systems Information Technologies-approved applied parts and accessories, is protected against defibrillator damage. NOTE: The electromagnetic compatibility profile of the V Monitor may change if accessories other than those specified for use with the V Monitor are used.
NOTE: The model of the monitor determines which symbols appear on it. Manufacturer: This symbol is accompanied by the name and the address of the manufacturer. Manufacturing Date: This symbol is accompanied by the date of the manufacturing.
European authorized representative. Packaging label depicting the transportation and storage atmospheric pressure range of to hPa. Please contact an authorized representative of the manufacturer for information concerning the decommissioning of your equipment. Vertically falling drops shall have no harmful effects to the Monitor. Any unauthorized attempt to repair equipment under warranty voids that warranty.
Failure on the part of the responsible individual, hospital or institution using this equipment to implement a satisfactory maintenance schedule may cause undue equipment failure and possible health hazards. Regular maintenance, irrespective of usage, is essential to ensure that the equipment will always be functional when required.
This manual is intended for service representatives and technical personnel who maintain, troubleshoot, or repair this equipment.
The V Monitor is intended to monitor one patient at a time in a clinical setting. Federal law U. To ensure patient safety, use only parts and accessories manufactured or recommended by GE Medical Systems Information Technologies. Parts and accessories used shall meet the requirements of EN Disposable devices are intended for single use only. They should not be reused. Periodically, and whenever the integrity of the monitor is in doubt, test all functions.
The warranty for this product is enclosed with the product in the shipper carton. All repairs on products under warranty must be performed or approved by Product Service personnel.
Unauthorized repairs will void the warranty. Only qualified electronics service personnel should repair products not covered by warranty. If the product fails to function properly, or if assistance, service or spare parts are required, contact Customer Support.
Before contacting Customer Support, it is helpful to attempt to duplicate the problem and to check all accessories to ensure that they are not the cause of the problem. If you are unable to resolve the problem after checking these items, contact GE Medical Systems Information Technologies. Prior to calling, please be prepared to provide:. If your product requires warranty, extended warranty or non-warranty repair service, call Customer Support and a representative will assist you.
To facilitate prompt service in cases where the product has external chassis or case damage, please advise the Customer Support representative when you call. Prior to returning any product for repair, you must have a RMA number. Remove all hoses, cables, sensors, and power cords from the monitor before packing. Pack only the accessories you are requested to return; place them in a separate bag and insert the bag and the product inside the shipping carton.
Place the product in a plastic bag and tie or tape the bag to prevent loose particles or materials from entering openings such as hose ports. Use a sturdy corrugated container to ship the product; tape securely to seal the container for shipping. Insurance is at the customer's discretion.
The shipper must initiate claims for damage to the product. A no charge rental unit is provided at no charge during the warranty period of the product when we perform the repair service. GE Medical Systems Information Technologies pays the shipping charges for a loaner sent to the customer for product repairs under the warranty. All loaners provided to customers must be returned within the specified time stated on the loaner agreement or a rental fee will be incurred.
Exchange replacement assemblies such as Circuit Board Assemblies also are available; ask the Customer Support representative for details. Please allow one working day for confirmation of your order. All orders must include the following information. As you use the V Monitor, you will accumulate solid wastes that require proper disposal or recycling.
These include batteries, patient applied parts, and packaging material. The sealed, rechargeable backup battery contains lead and can be recycled. The rechargeable memory battery is of the Sealed Lead Acid form. Discharge this battery prior to disposal. Place the battery in packaging which electrically isolates its contents.
Do not puncture or place the battery in a trash compactor. Do not incinerate the battery or expose it to fire or high temperatures. Dispose in accordance with regional body controlled guideline. Certain patient applied parts, such as those with adhesive disposable SpO 2. Other patient applied parts, such as blood pressure cuffs, should be cleaned according to instructions. Inspect reusable applied parts for wear, replace as necessary, and dispose of used product as medical waste in accordance with regional body controlled guideline.
Retain original packaging materials for future use in storing or shipping the Monitor and accessories. This recommendation includes corrugated shippers and inserts. Whenever possible recycle the packaging of accessories and patient applied parts. At the end of its service life, the product described in this manual, as well as its accessories, must be disposed of in compliance with the guidelines regulating the disposal of such products.
If you have questions concerning disposal of the product, please contact GE Medical Systems Information Technologies or its representatives. The V is for use on adult, pediatric, or neonatal patients—one at a time. The battery-operated monitor offers noninvasive determination of systolic blood pressure, diastolic blood pressure, mean arterial pressure, pulse rate, oxygen saturation, and temperature.
Monitors are available with or without integrated printers as well as the following parameters and technologies. Using the V Monitor, a clinician can measure, display, and record patient vital sign data that is derived from each parameter. All of the main operations of the V Monitor are easy-to-use and only a button-touch away. Please review the factory default settings and, where applicable, enter settings appropriate for your use. The contents of the pack vary according to model. Unpack the items carefully, and check them against the checklists enclosed within the accessory boxes.
If an accessory is missing or if an item is in a nonworking condition, contact GE Medical Systems Information Technologies Customer Service immediately. It is recommended that all the packaging be retained, in case the V Monitor must be returned for service in the future. Silence button: mutes audible alarms.
Any other active alarm that can be acknowledged is also removed whenever this key is pressed. When pressed, the silence icon bell lights red to indicate that audible alarms have been silenced for 2 minutes. Alarm silence can be cancelled by pressing the Silence button again. Alarms button: used to view or adjust parameter alarm limit settings.
When you reach the beginning or ending of a list, a negative key-click sounds. Refer to Operating Modes in this section for a description of clinical mode. SpO 2 sensor connector: attach SpO 2 cables here. Temperature probe holster: stores temperature probe. Temperature probe cover storage: stores probe covers. History button: activates the history mode to view stored patient data. The most recent entries are displayed first. Press and hold the button for 2 seconds to clear all entries stored; the adaptive inflate pressure setting returns to the configured setting.
Print button: prints currently displayed values or all stored entries when in history mode. Temperature probe connector: attach temperature probe cable here.
Silence icon: silences audible alarms for 2 minutes; silence icon bell lights. Pulse Rate window: shows pulse rate in beats per minute. Temperature window: lights 4-digit red LED to indicate measured temperature. Defibrillation protected.
When used with the recommended accessories, the monitor is protected against the effects of defibrillator discharge. If monitoring is disrupted by the defibrillation, the monitor will recover. Also evaluated to IEC No harmful effects will come of vertically falling drops of water making contact with the monitor. This section provides overall theory of operation and functional description of the V Monitor.
The V Monitor is a portable unit that receives power from an internal rechargeable Lead Acid Battery. The power regulators provide conditioned power from the Lead Acid Battery. Once the V Monitor is energized, a selftest is performed. The self-test automatically tests the main functions of the V Monitor. Failure of the self-test will set the V Monitor into a fail-safe mode with an audio alarm. Under normal operating conditions, the V Monitor is ready to record the patient vital signs using three external attachments: the temperature probe, SpO 2 sensor, and cuff.
Interface with a central station or other device is. Prior to each use, inspect the power supply cord to ensure proper connection and condition.
The SpO 2 probe has a built-in sensor. When the SpO 2 sensor is attached to the SpO 2 connector and patient, the probe senses both heart rate and oxygen saturation.
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