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Stryker LF2019 Instructions For Use Manual
Stryker LF2019 Instructions For Use Manual

Stryker LF2019 Instructions For Use Manual

Remanufactured ligasure exact dissector, without nano-coating

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Remanufactured by
Instructions for Use
Remanufactured LigaSure Exact Dissector, without Nano-coating
Caution: Federal (U.S.A.) law restricts this device to sale by or on the order of a physician.
Remanufactured Device for Single Use
• STERILE
• Exposed to Ethylene Oxide (EO) gas
VLFT10GEN SW v1.1 or Higher
LF2019
Compatible with:
Explanation of Symbols
Symbol
Standard
ISO 15223-
1:2016
ISO 15223-
1:2016
ISO 15223-
1:2016
ISO 15223-
1:2016
ISO 15223-
1:2016
ISO 15223-
1:2016
ISO 15223-
1:2016
ISO 15223-
1:2016
ISO 15223-
1:2016
ISO15223-
1:2016
ISO 7000:2019
Stryker Sustainability Solutions, Inc. ©2022
1810 W Drake Dr.
Tempe AZ, 85283
sustainability.stryker .com
888.888.3433
Registration
Symbol Title
Number
Sterilized using
2501
ethylene oxide
2497
Date of manufacture
2607
Use-by date
2493
Catalogue number
2492
Batch code
Consult instructions
1641
for use
1051
Do not re-use
2608
Do not resterilize
Do not use if package
2606
is damaged
Protect from
0626
moisture
3010
Contains RFID tag
Description
Indicates a medical device that has been sterilized
using ethylene oxide
Indicates the date when the medical device was
manufactured.
Indicates the date after which the medical device is
not to be used.
Indicates the manufacturer's catalogue number so that
the medical device can be identified.
Indicates the manufacturer's batch code so that the
batch or lot can be identified.
Indicates the need for the user to consult the
instructions for use.
Indicates a medical device that is intended for one use,
or for use on a single patient during a single
procedure.
Indicates medical device that is not to be resterilized.
Indicates a medical device that should not be used if
the package has been damaged or opened.
Indicates a medical device that needs to be protected
from moisture.
Indicates the presence of the RFID tag incorporated
within the packaging, container, or equipment without
identifying the specific air interface or data structure
employed.
Page 1 of 9

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Summary of Contents for Stryker LF2019

  • Page 1 Indicates the presence of the RFID tag incorporated within the packaging, container, or equipment without ISO 7000:2019 3010 Contains RFID tag identifying the specific air interface or data structure employed. Stryker Sustainability Solutions, Inc. ©2022 1810 W Drake Dr. Tempe AZ, 85283 sustainability.stryker .com 888.888.3433...
  • Page 2 Remanufactured LigaSure Exact Dissector, Without Nano-coating Page 2 of 9 The LF2019 is designed for use with Covidien electrosurgical generators that include vessel sealing capability. Please refer to Remanufactured LigaSure Exact Dissector, without Nano-coating Description the cover page for details on compatible generator models and software versions. If the software version on your generator is lower than required, contact Covidien about software updates.
  • Page 3 Remanufactured LigaSure Exact Dissector, Without Nano-coating Page 3 of 9 The safe and effect use of RF energy depends on many factors solely under the control of the operator. There is no substitute for properly trained and vigilant personnel. It is important that the operating instructions supplied with this or any other medical equipment be read, understood, and followed Use caution during surgical cases in which patients exhibit certain types of vascular pathology (atherosclerosis, aneurysmal Precaution...
  • Page 4 Examine all LigaSure system and instrument connections before using. Improper connections may result in arcing, sparks, Remanufactured LigaSure Exact Dissector, Without Nano-coating Page 4 of 9 accessory malfunction, or unintended surgical effects. Inspect the instrument and cords for breaks, cracks, nicks, or other damage before use. Failure to observe this caution may result in injury or electrical shock to the patient or surgical team or cause damage to the instrument.
  • Page 5 Do not divide tissue before the seal cycle is complete as this may result in improper sealing. Remanufactured LigaSure Exact Dissector, Without Nano-coating Page 5 of 9 Do not pull the cutting trigger while the jaws are open as injury to the patient or surgical team may occur. Conductive fluids (e.g., blood or saline) in direct contact with or in close proximity to the instrument may carry electrical current or heat, which may cause unintended burns to the patient.
  • Page 6 Remanufactured LigaSure Exact Dissector, Without Nano-coating Page 6 of 9 4. To seal adjacent tissue, overlap the edge of the existing seal. The second seal should be distal to the first seal to increase seal margin. A footswitch can be used instead of the hand-activation button (3). Ensure that the footswitch is connected to the footswitch Footswitch Activation receptacle that corresponds to the instrument receptacle in use.
  • Page 7: Troubleshooting

    Remanufactured LigaSure Exact Dissector, Without Nano-coating Page 7 of 9 The following is a list of troubleshooting suggestions for situations encountered when using the instrument with compatible Troubleshooting Covidien vessel sealing generators. For details on specific situations, refer to the corresponding generator user’s guide or the generator quick reference guide.
  • Page 8 Products for which Stryker is the Original Manufacturer Stryker warrants all products for which it is the original manufacturer, subject to the exceptions provided herein, to be free from defects in design, materials and workmanship and to substantially conform to the product specifications contained in the documentation provided by Stryker with the products for a period of one year from the date of purchase.
  • Page 9 (1) replace the product at no charge with a product that is at least functionally equivalent to the original product or (2) refund the purchase price of the product. If a refund is provided by Stryker, the product for which the refund is provided must be returned to Stryker and will become Stryker’s property.