SORIN GROUP SU-10101 Mode D'emploi page 5

DIRECTIONS FOR USE
1. For All Models
1.1 Remove the Suction Wand from the packaging using aseptic technique.
1.2 If provided, remove and discard the tip protector.
1.3 After removing the Suction Wand from the packaging, inspect the packaging and product for damage.
Do not use damaged product.
1.4 Flush the Suction Wand.
2. For Rigid, Flex-Tip and Low Profile Suction Wands
2.1 Connect the Suction Wand's 1/4" proximal connection to the suction line.
2.2 Using proper surgical technique, operate the Suction Wand to remove excess fluid from the surgical field.
3. For Flex-Tip and Low Profile Suction Wands
3.1 Fingertip must be placed over vent hole on the plastic handle of the Suction Wand to initiate full suction.
WARNING: Do not bend the tip excessively as this may kink the tip ceasing or reducing the suction.
WARNING: Care should be taken to apply only moderate force to the Suction Wand or Suction Wand's tip. Too
much pressure on the suction wand may cause the suction wand to bend or its tip to break.
4. For Rigid and Flex-Tip Suction Wands
4.1 Upon completion of the procedure, remove the suction wand from the suction line and discard it
properly.
5. Malleable and Flexible Suction Wand
NOTE: MALLEABLE SUCTION WAND MAY BE SHAPED BY FORMING IT. AVOID ABRUPT BENDS.
5.1 Using appropriate surgical technique, place the suction wand to the surgical field.
5.2 After proper placement of the suction wand, use proper surgical technique to secure the suction wand
to the surgical site.
5.3 Connect the Suction Wand's 1/4" proximal connection to the suction line.
6. For Malleable, Flexible and Low Profile Suction Wands
WARNING: Do not bend the Flexible Suction Wand Tubing excessively as this may kink the tubing ceasing or
reducing the suction.
WARNING: Suction tip requires monitoring and adjustment to assure safe positioning for proper drainage.
6.1 Upon completion of the procedure, remove the Suction Wand from the surgical field using proper
surgical technique. Disconnect it from the suction line and discard it properly.
WARNING: This device contains stainless steel. Do not use this device in a MRI environment.
7. For all Models
CAUTION: Federal (USA) law restricts this device to sale by or on the order of a physician.
DISPOSAL
Handle with care after use as the product may be contaminated with blood and/or body fluids. Dispose of
in accordance with applicable regulations in the country of use.
RETURN OF USED PRODUCTS
For Customers within the United States
If for any reason this product must be returned to Sorin Group USA, Inc. a returned goods authorization (RGA)
number is required from Sorin Group USA, Inc. prior to shipping.
If the product has been in contact with blood or body fluids, it must be thoroughly cleaned and disinfected before
packing. It should be shipped in either the original carton, or an equivalent carton, to prevent damage during
shipment; and it should be properly labeled with an RGA number and an indication of the biohazardous nature of
the contents of the shipment.
Instructions for cleaning and materials, including appropriate shipping containers, proper labeling, and an
RGA number may be obtained from the Sorin Group USA, Inc. Returned Goods Coordinator, Quality Assurance
Department (800-650-2623).
CAUTION
It is the responsibility of the health care institution to adequately prepare and identify the product for return shipment.
Do not return products that have been exposed to blood borne infectious diseases.
The shipping address for returned goods is:
Sorin Group USA, Inc.
Returned CV Products
14401 West 65th Way
Arvada, CO 80004-3599
For Customers Outside the United States
If for any reason this product must be returned, please contact your sales representative for specific instructions.
If the product has been in contact with blood or body fluids, it must be thoroughly cleaned and disinfected before
packing. It should be shipped in either the original carton, or an equivalent carton, to prevent damage during
shipment.
CAUTION
It is the responsibility of the health care institution to adequately prepare and identify the product for return shipment.
Do not return products that have been exposed to blood borne infectious diseases.
Sorin Group USA, Inc.
435085209 Rev A
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