Drive Medical Design AGF-602 manual SAFETY-TECHNICAL Controls, Malfunctions, Warranty

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4.Return the device to the carrying box with sponge foam to ensure that the unit is well-protected before transportation.

5.If the device is not to be used for a long period of time, remove the batteries from the battery compartment (acid may leak from used batteries and damage the device). Put the device and accessories in carrying box and keep it in cool dry place.

6.The packed TENS device should be stored and transported under the tem- pera ture range of -20¢J~ + 60¢J, relative humidity 20% ~ 95% , atmosphere pressure 500 hPa ~ 1060 hPa.

Chapter 20: SAFETY-TECHNICAL CONTROLS

For safety reasons, check your AGF-602 TENS each week based on the fol- lowing checklist.

1.Check the device for external damage.

-deformation of the housing.

-damaged or defective output sockets.

2.Check the device for defective operating elements.

-legibility of inscriptions and labels.

-make sure the inscriptions and labels are not distorted.

3.Check Led

-led must be illuminated when switched on.

4.Check the usability of accessories.

-patient cable undamaged.

-electrodes undamaged.

Please consult your distributor if there are any problems with device and accessories.

Chapter 21 MALFUNCTIONS

Should any malfunctions occur while using the TENS, check

-whether the switch/control is set to the appropriate form of therapy. Adjust the control correctly.

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-whether the cable is correctly connected to the device. The cables should be inserted completely into the sockets.

-whether the impulse display led is illuminated. If necessary, insert a new battery.

-for possible damage to the cable. Change the cable if any damage is detected. * If there is any other problem, please return the device to your distributor. Do

not try to repair a defective device.

Chapter 22 Conformity to Safety Standards

STATEMENT OF EMC

The AGF-602 TENS devices are in compliance with IEC 60601-1-2: 1993.

CONFORMITY TO MDD REQUIREMENTS

The AGF-602 TENS devices are in compliance with

IEC60601-1 safety standard and FDA 510K standards.

Chapter 23 : WARRANTY

All AGF-602 TENS models carry a warranty of three year from the date of delivery. The warranty applies to the stimulator only and covers both parts and labour relating thereto.

The warranty does not apply to damage resulting from failure to follow the operating instructions, accidents, abuse, alteration or disassembly by un- authorized personnel.

Manufacturer:

MEDICAL DEPOT INC DBA DRIVE MEDICAL

99 Seaview Boulevard

Port Washington, NY 11050

Phone # : 516-998-4600

Edition : V1.1

Printed in February , 2007

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Contents Port Washington, NY Index HOW Tens Works IntroductionExplanation of Pain Explanation of TensConstruction General DescriptionReplacable Parts Technical SpecificationsAccessories Parameter Controls Graphic SymbolsElectrode Options Attachment of Electrode Lead WiresLead Wire Maintenance Electrode PlacementApplication of RE-USABLE Self Adhesive Adjusting the ControlsPage Rechargeablebatteries Battery InformationMAINTENANCE, Transportation BatterychargingMalfunctions SAFETY-TECHNICAL ControlsConformity to Safety Standards Warranty