Stryker LF2019 Instructions For Use Manual Download Page 1

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Remanufactured by

Instructions for Use
Remanufactured LigaSure Exact Dissector, without Nano-coating

Remanufactured Device for Single Use

Caution: Federal (U.S.A.) law restricts this device to sale by or on the order of a physician.

•

STERILE

•

Exposed to Ethylene Oxide (EO) gas

LF2019 Compatible with:

VLFT10GEN SW v1.1 or Higher

Explanation of Symbols

Symbol

Standard

Registration

Number

Symbol Title

Description

ISO 15223-

1:2016

2501

Sterilized using

ethylene oxide

Indicates a medical device that has been sterilized

using ethylene oxide

ISO 15223-

1:2016

2497

Date of manufacture

Indicates the date when the medical device was

manufactured.

ISO 15223-

1:2016

2607

Use-by date

Indicates the date after which the medical device is

not to be used.

ISO 15223-

1:2016

2493

Catalogue number

Indicates the manufacturer’s catalogue number so that

the medical device can be identified.

ISO 15223-

1:2016

2492

Batch code

Indicates the manufacturer’s batch code so that the

batch or lot can be identified.

ISO 15223-

1:2016

1641

Consult instructions

for use

Indicates the need for the user to consult the

instructions for use.

ISO 15223-

1:2016

1051

Do not re-use

Indicates a medical device that is intended for one use,

or for use on a single patient during a single

procedure.

ISO 15223-

1:2016

2608

Do not resterilize

Indicates medical device that is not to be resterilized.

ISO 15223-

1:2016

2606

Do not use if package

is damaged

Indicates a medical device that should not be used if

the package has been damaged or opened.

ISO15223-

1:2016

0626

Protect from

moisture

Indicates a medical device that needs to be protected

from moisture.

ISO 7000:2019

3010

Contains RFID tag

Indicates the presence of the RFID tag incorporated

within the packaging, container, or equipment without

identifying the specific air interface or data structure

employed.

1810 W Drake Dr.

Tempe AZ, 85283

sustainability.stryker .com

888.888.3433

Summary of Contents for LF2019

Page 1: ...entified ISO 15223 1 2016 2492 Batch code Indicates the manufacturer s batch code so that the batch or lot can be identified ISO 15223 1 2016 1641 Consult instructions for use Indicates the need for the user to consult the instructions for use ISO 15223 1 2016 1051 Do not re use Indicates a medical device that is intended for one use or for use on a single patient during a single procedure ISO 152...

Page 2: ... and division of vessels lymphatics and tissue bundles 2 3 mm away from unintended thermally sensitive structures such as nerves and parathyroid glands The LigaSure system has not been shown to be effective for tubal sterilization or tubal coagulation for sterilization procedures Do not use the LigaSure system for these procedures Contraindications for Use The LigaSure system has not been shown to...

Page 3: ...ach side arrow shows direction for cutting Cable cord Connector purple and white Precaution The nano coating featured on the original device is not present on this product Adjunctive use of nerve monitoring device is recommended during nerve sparing procedures such as thyroidectomies radical neck dissection and parotidectomies Secondary hemorrhaging after tonsillectomy is a potentially serious adv...

Page 4: ...nerator Refer to the generator user s guide for additional set up information During Surgery The LigaSure Sealer Divider can be used during surgery both to manipulate and dissect tissue and to seal and cut vessels and tissue bundles Instructs for use of the instrument during a procedure are provided in this section Warning Avoid placing fingers between the jaws or ring handles Injury to the use ma...

Page 5: ...the system only when the instrument is in direct contact with the target tissue to lessen the possibility of unintended burns Do not activate the instrument while instrument jaws are in contact with or in close proximity to other instruments including metal cannulas as localized burns to the patient or physician may occur Eliminate tension on the tissue when sealing and cutting to ensure proper fu...

Page 6: ...ssel or tissue After inspecting the seal the surgeon should create a second seal adjacent to the first seal before cutting as described below A tone with multiple pulses indicates that the seal cycle was not completed Refer to the Troubleshooting section for possible causes and corrective actions Do not cut tissue until you have verified that there is an adequate seal 6 To seal adjacent tissue ove...

Page 7: ... The user is grasping thin tissue or not enough tissue open the jaws and confirm that a sufficient amount of tissue is inside the jaws If necessary increase the thickness of the tissue that is grasped and reactivate the seal cycle Too much tissue between the jaws The user is grasping too much tissue open the jaws reduce the amount of tissue tat is grasped and reactivate the seal cycle Activating o...

Page 8: ...of one year from the date of purchase General Warranty Terms Applicable to All Products TO THE FULLEST EXTENT PERMITTED BY LAW THE EXPRESS WARRANTY SET FORTH HEREIN IS THE ONLY WARRANTY APPLICABLE TO THE PRODUCTS AND IS EXPRESSLY IN LIEU OF ANY OTHER WARRANTY BY STRYKER EXPRESSED OR IMPLIED INCLUDING BUT NOT LIMITED TO ANY IMPLIED WARRANTY OR MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE IN ...

Page 9: ...he initial warranty period has expired by the time the product is repaired or replaced for thirty 30 days after delivery of the repaired or replaced product When a product or component is replaced the item provided in replacement will be the customer s property and the replaced item will be Stryker s property If a refund is provided by Stryker the product for which the refund is provided must be r...

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