Zimmer Biomet PULSAVAC PLUS 00-5150-420-00 Manual Del Usuario

ENGLISH
PULSAVAC
WOUND DEBRIDEMENT
SYSTEM
REF 00-5150-420-00 – The Component Kit Pack includes the Pulsavac Plus Handpiece and all
required tubing.
REF 00-5150-475-00 – The Fan Spray Kit Pack includes the Pulsavac Plus Handpiece, all
required tubing, and a High Capacity Fan Spray Debridement Tip.
REF 00-5150-482-00 – The Hip Kit Pack includes the Pulsavac Plus Handpiece, all required tubing,
High Capacity Fan Spray Debridement Tip, and a High Capacity Narrow Intramedullary Tip.
REF 00-5150-495-00 – The Shower Spray Kit Pack includes the Pulsavac Plus Handpiece, all
required tubing, and a High Capacity Shower Spray Debridement Tip.
Sterile only if package is unopened and undamaged.
INDICATIONS FOR USE:
Pulsatile Lavage and removal of debris from operative area
FUNCTIONS:
• Debridement of a wound site through irrigation and suction
• Preparation of a bone bed prior to cementing a joint
KNOWN CONTRAINDICATIONS
None Known
CAUTION:
Use of a Y-Connector Set with a diameter less than 0.095" (2.4mm) may diminish the functional
performance of the device and cause premature failure of the device. Zimmer recommends the
use of the 00-5150-042-00, Dual Spike Y-Connector Set.
WARNINGS:
Explosion hazard. Do not use in presence of flammable anesthetics or gases.
No modification of this equipment is allowed.
Do not submerge handle in liquid as this may compromise the efficiency of the pump or alter the
pH of the liquid.
Do not cut the battery pack cable. Cutting through the battery pack cable could lead to shock,
excessive heat and/or sparks, and could result in fire and/or personal injury.
Do not submerge the battery pack in liquid.
Use caution when removing batteries. The battery pack contains alkaline batteries. Exposure to
the contents of an open or leaking battery or their combustion products could be harmful. Avoid
skin and eye contact. Use neoprene or natural rubber gloves and safety glasses with side shields
when handling batteries.
The Batteries Directive 2006/66/EC introduces new requirements from September 2008 on
removability of batteries from waste equipment in EU Member States. To comply with this
Directive, this device has been designed for safe removal of the batteries at end-of-life by a waste
treatment facility. Infected units should be de-contaminated before they are sent for recycling. In
the case that it is not possible to decontaminate the unit for recycling, the hospital should not
attempt to remove the batteries from waste equipment. Continued disposal of small amounts of
portable batteries to landfill and incineration is allowed under the Batteries Directive 2006/66/EC
and Member State regulations.
Reuse of a single use device that has come in contact with blood, bone, tissue or other body
fluids may lead to patient or user injury. Possible risks associated with reuse of a single use
device include, but are not limited to, mechanical failure and transmission of infectious agents.
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PLUS
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