portable ac/dc suction pump USER’S MANUAL ITEM # 18605
index 1. 2. 3. 4. 5. 6. 7. 8. 8. 9. 10. 11. 12. 1 Safety Information..........................................................2-4 AC Power Source.............................................................3 Electrical............................................................................3-4 Introduction.......................................................................4 Illustration of Important Parts......................................5 Set-Up.................................................
safety information 2 1. SAFETY INFORMATION When using electrical products, especially when children are present, basic safety precautions should always be followed. Read all instructions before using. Important information is highlighted by these terms: DANGER Urgent safety information for hazards that will cause serious injury or death. ! WARNING Important safety information for hazards that might cause serious injury. ! ! CAUTION Information for preventing damage to the product.
safety information 3 ! SPECIFIC WARNINGS TO REDUCE THE RISK OF ELECTRICAL SHOCK OR INJURY TO PERSONS, DO NOT DISASSEMBLE THIS UNIT. DISASSEMBLY OR ATTEMPTED REPAIRS IF ACCOMPLISHED INCORRECTLY CAN CREATE ELECTRICAL SHOCK HAZARD. ONLY QUALIFIED TECHNICIANS SHOULD PERFORM SERVICING OF THIS SUCTION UNIT. ! DANGER The AC/DC Portable Suction Pump is a vacuum suction device designed for the collection of nonflammable fluid materials in medical applications only.
safety information ! WARNING Proper operation of this product is necessary to avoid physical harm. Improper use can cause personal injury and/or tissue damage. This product should not be used unless the operator has been instructed by a physician or other qualified health care professional. introduction Features: New anti-bacteria filter design helps prevent contamination. High quality vacuum regulator and anti-vibration vacuum gauge setting. Oil-less, permanent lubrication.
illustration of important parts 5 Item # 18605 1. Bacteria filter (non-sterile) 2. 4” Connection tubing 3. Vacuum gauge 4. Tubing connector 5. Vacuum regulator knob 6. DC power input (on side) 7. Power switch 8. 6’ patient tubing 9. 800 cc disposable canister w/lid (float shut off incorporated into lid) 10.
set up & operation 6 IMPORTANT OPERATION AND BATTERY INSTRUCTIONS: Your 18605 portable suction machine is capable to run on AC or DC power. To ensure full function of this unit, the battery must be completely charged before the first use. Do not turn on the unit before the battery is completely charged. It takes approximately 1.5 hours to fully charge the unit. Charge the unit when battery levels are low to ensure proper operation. 1.
set up & operation 7 BATTERY OPERATION: To ensure proper operation from internal battery, fully charge the battery for 1.5 hours as explained in the Battery Charging section. To operate the unit from an internal rechargeable battery, ensure that no external power sources are plugged into the DC power input on the side of the unit. Once the power source is selected, simply turn the unit on using the power switch located on the side of the unit.
cleaning & maintenance 8 BATTERY CHARGING On 18605 series, the units are equipped with a factory-installed rechargeable battery. The unit will have a light for low battery and charge indication. Once you’ve determined that your unit is equipped with an internal rechargeable battery, connect the unit to the proper AC or DC power source using the AC adapter or DC power cord. The yellow charge indicator will be illuminated while the battery is charging.
cleaning &maintenance 9 Collection Bottle: 1. Shut off unit using power switch and allow vacuum to drop. Disconnect power source from the DC input receptacle on the unit. 2. With the collection bottle still in the holder, remove the lid. The bottle can now be taken out of the holder to be emptied. NOTE Collection bottle should be emptied and cleaned after each use. The 800ml disposable collection bottle and lid are meant for single-patient use 3.
maintenance & troubleshooting 10 MAINTENANCE Inspect suction tubing and collection bottle for leaks, cracks, etc. before each use. DANGER Electric shock hazard. Do not attempt to open or remove cabinet, there are no user-serviceable internal components. If service is required, return unit to a qualified Drive Medical provider or an authorized service center. Opening or tampering with the unit will void warranty. Filter Changing: 1.
specifications / classification 11 Size H x W x D inches (cm) . . . . . . . . . . . . . . . . . . . . . . . . . . . .14.2 x 7.0 x 8.0 (36 x 17.8 x 20.3) Weight lb. (kg.) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7.3 lbs (3.3 kg) Electrical Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 100-240 V AC 50/60 Hz .1.2 A max; 12 V DC, 36 W max Internal Rechargeable Battery. . . . . . . . . . . . . . . . . . . . . . . . .
specifications / classification 12 APPROVALS 18605 Series . . . . . . . . . . . . . . . . . . . . . . . . . . . .IEC 601-1; CAN/CSA-C22.2 No. 601.1-M90; UL 60601-1, EN 60601-1-2 18605 meets RTCA/D-160D . . . . . . . . . . . . . . . . . . . . . . . . .DO-160D - section 21 Category M EQUIPMENT CLASSIFICATIONS With respect to protection from electric shock . . . . . . . . . . . .Class I and internally powered Degree of protection against electric shock . . . . . . . . . . . . . .
warranty 13 TWO-YEAR LIMITED WARRANTY The compressor portion of the Drive Suction Unit 18605 Series (excluding internal rechargeable batteries) is warranted to be free from defective workmanship and materials for a period of two years from date of purchase. Internal rechargeable batteries are warranted for 90 days. Any defective part(s) will be repaired or replaced at Drive Medical’s option if the unit has not been tampered with or used improperly during that period.
warranty 14 DECLARATION OF CONFORMITY Manufacturer: Drive Medical Design & Manufacturing 99 Seaview Boulevard Port Washington, NY 11050 Product Designation : Type/Model: 18605 We herewith declare that the above-mentioned product complies with the requirements of EC Directive 93/42/EEC and the following: Class: IIa, Rule 2 Quality System Standards Applied: IS09001/ISO13485 Notified Body RWTUV MDD Annex II Applied Safety Standards Applied: EN60601-1/IEC 601-1:1988 including A1:1991 and A2:1995 CAN/CSA 22.
Drive Medical Design & Manufacturing 99 Seaview Boulevard Port Washington, NY 11050
