Yasargil Permanent Aneurysm Clips

Similar documents
Instructions for use 0483 Permanent and temporary YASARGIL Aneurysm and Vessel Clips

Aesculap Implant Systems

DISTAL RADIUS. Instructions for Use

Aesculap Spine Instructions for use

PRO-DENSE Bone Graft Substitute The following languages are included in this packet:

PRO-DENSE BONE GRAFT SUBSTITUTE

Aesculap CranioFix absorbable

For the Attention of the Operating Surgeon: IMPORTANT INFORMATION ON THE MATRIXRIB FIXATION SYSTEM

JRI Thompson Hemiarthroplasty

Aesculap CeSpace TM PEEK and CeSpace TM XP Spinal Implant System Instructions for Use

Manufacturer s information

Revision A Date:

METAL HEMI SYSTEM

EasyStep. Operative technique

External Distal Radius Fixator. Supplement to the 8 mm rod fixator system

Device Preparation (all steps to be performed per standard interventional technique)

EVOLVE TRIAD BONE SCREWS

Velocity Orthopedics Instrument Cleaning and Sterilization

Cochlear Implants. Medical Procedures. for MED EL CI Systems. AW33290_5.0 (English US)

SIDEKICK EZ FRAME EXTERNAL FIXATION SYSTEM The following languages are included in this packet:

MRI GUIDELINES FOR INSPIRE THERAPY

The following languages are included in this packet:

Reprocessing Guide. Autoclavable Arthroscope and Hardware Sterilization Tray

Cochlear Implants. Medical Procedures. for MED EL Implant Systems. AW33290_2.0 (English US)

1.5 Tesla and 3 Tesla Magnetic Resonance Imaging (MRI) Guidelines for the Senza System (IPG1000 and IPG1500)

Instructions for use Prodisc -C Vivo Cervical disc prosthesis

1.5 Tesla and 3 Tesla Magnetic Resonance Imaging (MRI) Guidelines for the Senza System (IPG1000 and IPG1500)

TC-PLUS Primary Knee IMPORTANT MEDICAL INFORMATION SPECIAL NOTE. This Package Insert is for product distributed in the US only.

INSTRUCTIONS FOR USE AND CARE

VNS Therapy System Physician s Manual

LOW PROFILE NEURO. This publication is not intended for distribution in the USA. SURGICAL TECHNIQUE

For use by an Accredited Orthopaedic Surgeon only

Low-Profile Wrist Fixator. For stabilization of fractures of the distal radius.

S5 Rotary Files. only. Manufacturer. Packing unit. Batch code. For professional use only (0)

ProUltra Ultrasonic Non Surgical Endo Tips

Low Profile Neuro Plating System. Surgical Technique

Lotus transducer Instructions for use

Micra MC1VR01. MRI procedural information for Micra Model MC1VR01 MR Conditional single chamber transcatheter pacing device (VVIR)

FastFrame External Fixation System. Damage Control Surgical Technique

Warning: Patients should not be exposed to MRI environments until the surgical site following pump implantation is fully healed.

Customized Cranial and Craniofacial Implants. Instructions For Use. 7000revD_Instructions_For_Use. Page 1 of 8

EVOLVE TRIAD SYSTEM

Metallic Internal Fixation Devices The following languages are included in this packet:

Aesculap CranioFix 2. Cranial fixation system. Aesculap Neurosurgery

Ceramic Femoral Heads and Acetabular Cup Liners

St. Jude Medical 8-Channel Adapter. Clinician's Manual

OPERATIVE TECHNIQUE. CONSTRUX Mini PTC. Mini PTC Spacer System

REBEL. Platinum Chromium Coronary Stent System. Patient Information Guide

The A-Space SIBD Spinal System is a stand-alone device intended to be used with the four supplied bone screws if no supplemental fixation is used.

Headless Compession Screw 2.5 / 3.0

MRI GUIDELINES FOR INSPIRE THERAPY

Read this manual before performing an MRI scan on a patient implanted with an Algovita Spinal Cord Stimulation System.

Medium External Fixator Humeral Shaft Frame. Modular frame for upper extremity use.

Algovita. MRI Procedure Guidelines. Spinal Cord Stimulation System. 201x

DARCO MIS FOREFOOT SCREW

Lapidus Arthrodesis System Instructions for Use

ProUltra ULTRASONIC SURGICAL TIPS

Altus Product description / Instructions for Use IFU 6 Rev. 1

Medium External Fixator Pediatric Femoral Shaft Frame. Using medium multi-pin clamps.

CELLPLEX TCP SYNTHETIC CANCELLOUS BONE

UNICLIP DIRECTIONS FOR USE REF C226U - 0,8 MM / 1 MM FOR DENTAL USE ONLY. FISDR / F EN / 11 / updated 06/2016 1/7

Technique Guide KISSloc Suture System

Single Use Curlew TM Multiple Biopsy Forceps

X-spine Systems, Inc. Silex Sacroiliac Joint Fusion System

DISCLAIMER OF WARRANTY AND LIMITATION OF REMEDY

MRI-Ready Systems Manual. MRI Procedure Information for the St. Jude Medical MR Conditional System

AS Medizintechnik GmbH Sattlerstraße Tuttlingen Germany

Headless Compession Screw 4.5 / 6.5 SURGICAL TECHNIQUE. Titanium or Stainless Steel. Cannulated Headless Design. Multiple Thread Options.

REFILL KIT For use with Prometra Programmable Infusion Systems

AXS Catalyst Distal Access Catheter

Carry this card with you at all times. Show this card to any medical professional treating you. Patient Implant Card. Option ELITE Vena Cava Filter.

TriboFit Hip System. Issue 3 - August 2013 English

Patient Brochure. Clearstream Technologies, Ltd. Moyne Upper Enniscorthy Co. Wexford, Ireland. PK Rev. 0 05/17

The following languages are included in this packet:

X-spine Systems, Inc. Axle Interspinous Fusion System

X-spine Systems, Inc. Irix-A Lumbar Integrated Fusion System

STERILE IMPLANT PRODUCT INSERT PATIENT-FITTED TEMPOROMANDIBULAR JOINT RECONSTRUCTION PROSTHESIS SYSTEM

Page 1 of 7 Doc. No.: IU/15 Rev. No.: 05 Rev. Date:03MAY2018. Instructions for use for ATLAS Tibial Fracture(TF) Nail

ENDO-FUSE INTRA-OSSEOUS FUSION SYSTEM The following languages are included in this packet:

Desara TV and Desara Blue TV

Aesculap Implant Systems

low ProfIle neuro PlaTIng system

MRI Safety Information for the HiRes Ultra 3D Cochlear Implant

SYMBOLOGY. = Manufacturer. = Manufacturing Serial Number. = Manufacturing Lot Number = Catalog Number LOT REF. = Do not resterilize Single Use Only

Preparation Instructions for the CAMLOG /CONELOG Implant System

Amendia Interbody Fusion Devices PACKAGE INSERT

Safety Issue of Static Magnetic Field (1)

Doc no: IFU/CPL Issue date: Rev no: 00 Rev date: 1

Document No Rev. B Pg. 1 of 5 Approvals / Date Title: INSTRUCTIONS FOR USE DJO SURGICAL MODULAR REVISION HIP SYSTEM AND ACETABULAR CAGE

X-spine Aranax Anterior Cervical Plating System Instructions for Use / Package Insert

OBSOLETE. Visit for the latest version. Ankle Plating System 3 PKGI-79-B EFFECTIVE

M6-C Artificial Cervical Disc Surgical Instruments

Hygienic Reprocessing

X-spine Systems, Inc. Calix PC Spinal Implant System

8 Performing Medical Procedures

EXTERNAL FIXATION SYSTEMS The following languages are included in this packet:

The SplitWire Percutaneous Transluminal Angioplasty Scoring Device. Instructions for Use

Table of Contents. Introduction Indications For Use Contraindications Warnings Precautions...5

VariAx Compression Plating System. Operative technique

Transcription:

Yasargil Permanent Aneurysm Clips Yasargil aneurysm clips Figure captions 1 Yasargil Phynox aneurysm clip, example of a straight clip 2 Yasargil titanium aneurysm clip, example of a straight clip 3 Yasargil aneurysm clip, correctly positioned 4 Yasargil aneurysm clip, incorrectly positioned 5 Yasargil aneurysm clip, incorrectly positioned 6 Yasargil aneurysm clip, incorrectly positioned Legend A Test point B Force C Length of jaw part

Symbols on product and packages Sterilization using radiation Not for reuse in intended applications as defined by the manufacturer Use by Attention, see instructions for use INDICATIONS FOR USE The Yasargil Aesculap Aneurysm Clips are intended for occlusion of cerebral aneurysms in a permanent manner. They are applied with Aesculap clip appliers, which contain titanium alloy or phynox jaws. Aesculap Yasargil aneurysm clips will be referred to as aneurysm clips in the following text. Permanent aneurysm clips The permanent aneurysm clips are intended for permanent stasis of cerebral aneurysms. The permanent aneurysm clips are intended for single use only. CONTRAINDICATION The permanent aneurysm clips are contraindicated for all applications except for the permanent stasis of cerebral aneurysms. WARNINGS Each aneurysm clip is individually packaged and provided sterile and is intended for use on a single patient during a single procedure. AESCULAP recommends sterile presentation to the operative field to ensure the integrity and performance of the clip and to ensure accurate retention of implant information on intraoperative records. Permanent aneurysm clips are indicated for permanent occlusion of aneurysms and, therefore, repeated or multiple application during the procedure should be avoided. Any aneurysm clip that has come in contact with a patient's blood or bodily fluid should not, under any circumstances, be cleaned, re-sterilized or in any other way prepared for use in another patient. PRODUCT DESCRIPTION The aneurysm clips are available in two different materials: Cobalt alloy (Phynox) ISO 5832-7 and Titanium alloy Ti6Al4V, ISO 5832-3.

Different models of aneurysm clips are available. Please contact your local Aesculap sales representative for more information or consult the Yasargil Aneurysm brochure located at www.aesculapusa.com. The aneurysm clips are available in three sizes (Mini, Standard and Long). The closing force of each aneurysm clip is measured individually and printed on the individual packaging. The closing force given on the packaging was measured at 1/3 along the length (from the tip) of the jaw part, at the center of the contact area. The Phynox aneurysm clips are measured with the jaws opened to 0.5 mm (see Fig. 1) whereas the titanium aneurysm clips are measured with the jaws opened to 1 mm (see Fig. 2). Each aneurysm clip carries an individual serial number. The aneurysm clips are color-coded to differentiate the various sizes and applications. Special product description for permanent aneurysm clips Each permanent aneurysm clips package contains additional labels showing the article number and the individual serial number of the clip. MRI Safety Information MR Conditional The Yasargil Titanium Aneurysm Clips are MR Conditional. Non-clinical testing demonstrated that the Yasargil Titanium Aneurysm Clips are MR Conditional. A patient with this device can be safely scanned immediately after implantation in an MR system meeting the following conditions: Static magnetic field of 3-Tesla or less Maximum spatial gradient magnetic field of 3,000-Gauss/cm (30.0 T/m) or less Maximum MR system reported, whole body averaged specific absorption rate (SAR) of 4-W/kg (First Level Controlled Operating Mode) Do not take the aneurysm clip applier into the MR environment. It is MR Unsafe. Under the scan conditions defined above, the Yasargil Titanium Aneurysm Clip is expected to produce a maximum temperature rise of +1.8 C after 15 minutes of continuous scanning. In non-clinical testing, the image artifact caused by the device extends approximately 5 mm from the Yasargil Titanium Aneurysm Clip when imaged with a gradient echo pulse sequence and a 3-Tesla MR system.

MRI Safety Information MR Conditional The Yasargil Phynox Aneurysm Clips are MR Conditional. Non-clinical testing demonstrated that the Yasargil Phynox Aneurysm Clips are MR Conditional. A patient with this device can be safely scanned immediately after implantation in an MR system meeting the following conditions: Static magnetic field of 3-Tesla or less Maximum spatial gradient magnetic field of 1,500-Gauss/cm (15.0 T/m) or or less Maximum MR system reported, whole body averaged specific absorption rate (SAR) of 4-W/kg (First Level Controlled Operating Mode) Do not take the aneurysm clip applier into the MR environment. It is MR Unsafe. Under the scan conditions defined above, the Yasargil Phynox Aneurysm Clip is expected to produce a maximum temperature rise of +2.2 C after 15 minutes of continuous scanning. In non-clinical testing, the image artifact caused by the device extends approximately 20mm from the Yasargil Phynox Aneurysm Clip when imaged with a gradient echo pulse sequence and a 3-Tesla MR system. Safe handling and preparation CAUTION Federal law restricts this device to sale by or on order of a physician! Read and observe the instructions for use, and keep them in a safe place. The product may only be used for its intended application, see Indications for Use. Prior to each use, inspect the product for: loose, bent, broken, cracked, worn, or fractured components. Do not use the product if it is damaged or defective. Products found to be damaged must be set aside immediately. Each aneurysm clip is individually packaged and sterilized by radiation (min. dose 25 kgy). If the sterile wrapping is open, torn, perforated or otherwise damaged, or when the sterility of the aneurysm clip has expired (use-by date), the aneurysm clip must be regarded as unsterile and has to be sterilized according to the instructions given in the sections on cleaning and sterilizing. Each individually packaged aneurysm clip is supplied in double sterile packaging including instructions for use and labels. Special handling and preparation for permanent aneurysm clips Aesculap recommends keeping the permanent aneurysm clips in the unopened sterile packaging, prior to operation. In this way, damage to the aneurysm clips is avoided, their functionality is ensured and their correct closing force is maintained.

Labels Each permanent aneurysm clip package contains additional labels showing the article number and the individual serial number of the clip. To facilitate the subsequent radiological examination, the patient s file (for the hospital) and the patient ID (for the patient) should be marked with these labels. Patient ID Important information concerning the aneurysm clip implanted and the operation can be noted down on the patient ID. To facilitate the postoperative radiological examination, each patient should receive a patient ID. Contents of the patient ID Patient data Hospital data Date of operation Name of surgeon Article number and individual serial number of the aneurysm clip implanted The patient ID can be ordered through your Aesculap sales representative. Patients should register the conditions under which the implant can be scanned safely with the MedicAlert Foundation (www.medicalert.org) or equivalent organization. To avoid damage, product malfunction or to avoid any risk of a decrease closing force: Apply each aneurysm clip with the appropriate applier and removal forceps. Never use the aneurysm clips with applier or removal forceps from other manufacturers. The Phynox aneurysm clips must be applied with the applier for Phynox aneurysm clips. The titanium aneurysm clips must be applied with the applier and removal forceps for titanium aneurysm clips. Mini, Standard or Long aneurysm clips may be used only with the applier and removal forceps of the appropriate size (Mini, Standard or Long). All applier and removal forceps are marked according to size (Mini, Standard or Long) and clip material so that their correct application with clips of the respective size and material is ensured. Additionally, the applier and removal forceps for titanium aneurysm clips can also be color-coded according to clip size.

For further information on the suitable applier and removal forceps, please contact your local Aesculap sales representative or consult the Yasargil Aneurysm Clip Brochure which can be located at www.aesculapusa.com. Carefully pick up the whole aneurysm clip with the jaw piece of the appropriate applier forceps (see Fig. 3). The aneurysm clip can be damaged, jump out or slip if picked up improperly (see Fig. 4/5/6). To avoid possible risks to the patient: The permanent aneurysm clips are designed for single use only. Aesculap cannot accept any responsibility for aneurysm clips that are handled inappropriately or not according to the present instructions for use. Safe handling Aneurysm clips should only be applied by surgeons appropriately trained for, and experienced in, the use of aneurysm clips. If an aneurysm clip appears changed or shows signs of damage, e.g. incorrect jaw position, bent parts or changed closing force: Set aside the aneurysm clip. To avoid damage to the aneurysm clips: Always handle the aneurysm clips with appropriate care. Never open an aneurysm clip with your fingers. Avoid manual and/or mechanical manipulation of the aneurysm clip. Excessive, rough or repeated handling, especially opening and closing of aneurysm clips, be it in general use or during cleaning and sterilization, can change the closing force and impair the clinical effectiveness of the aneurysm clips. As soon as the sterile aneurysm clip has been brought to the operation field in the usual manner, pick up the aneurysm clip from its double sterile packaging and position it carefully between the jaws of the applier forceps. The correct positioning of the aneurysm clip between the jaws of the appropriate applier forceps (see Fig. 3) is crucial here. If the aneurysm clip is not placed precisely between the jaws parts of the appropriate applier forceps (see Fig. 4/5/6), this can lead to damage to the aneurysm clip. It could cause a change in the factory-set closing force or result in the aneurysm clip slipping from the applicator, which could be dangerous during an operation. These directions for use must also be observed when using the removal forceps. To preclude the possibility of a galvanic reaction; avoid implanting permanent aneurysm clips made of different materials and/or by different manufacturers in such a way that they touch each other. Make absolutely certain that the aneurysm clip sits correctly on the aneurysm neck and close to the blood vessel, during and after implantation.

The application of aneurysm clips involves the following severe risks: Shifting or breakage of the aneurysm clip. Scissoring of the jaw. Rupture of the aneurysm due to punctual, incomplete contact of the clip jaws on the aneurysm neck. For large aneurysms, reduction of the blood vessel crosssection close to the edge of the blood vessel. Cerebrovascular spasms and sudden death. Infections of the operation wound and general surgical complications are other unwelcome (side) effects. Each patient must be informed comprehensively about the properties of aneurysm clips, the surgical procedure and the importance of the medical id cards.. Care and handling Each aneurysm clip in its unopened original packaging has been packed and sterilized individually and is supplied as a sterile product. Sterilization of a clip that has been removed from its sterile package may be accomplished by the following sterilization process outlined in the following section. To preclude damage, inaccurate functioning and an incorrect closing force: Use each aneurysm clip with the appropriate applier and removal forceps. Never use the aneurysm clips with applier or removal forceps from other manufacturers. Excessive, rough or repeated handling, especially opening and closing of aneurysm clips, be it in general use or during cleaning and sterilization, can damage the aneurysm clip, change the closing force and impair the clinical effectiveness of the aneurysm clips. To avoid damage to the aneurysm clips: Always handle the aneurysm clips with appropriate care. Never open an aneurysm clip with your fingers. Avoid manual and/or mechanical manipulation of the aneurysm clip. Permanent aneurysm clips that have been implanted before or been in contact with blood, tissue, or body fluids: Must be set aside for disposal. Must not be sterilized.

Cleaning and disinfection Special cleaning instructions for permanent aneurysm clips Sterilization must be preceded by the following procedure: Mechanical alkaline cleaning and thermal disinfecting Machine type: single-chamber cleaning/disinfection device without ultrasound Phase Step T t Water- Chemical/Remarks [ C/ F] [min] Quality I Prerinse < 25/77 3 D W - II Cleaning 55/131 10 FD W Concentrate, alkaline: ph = 13 <5 % anionic surfactant 0.5 % working solution ph = 11 III IV Intermediate rinse Thermal disinfecting >10/50 1 FD W - 90/194 5 FD W - V Drying - According to the program for cleaning and disinfection device D W: Drinking water FD W: Fully desalinated water (demineralized, low microbiological contamination: drinking water quality at least) Check visible surfaces for residues after mechanical cleaning/disinfecting. Inspection Inspect each individual aneurysm clip. Any aneurysm clip found with one of the following characteristics must be set aside and excluded from further use: Signs of damage Incorrect jaw position Bent components Changed closing force Misalignment Soilage that cannot be removed The color coding may fade in the course of processing. Aneurysm clips whose color coding cannot be identified unambiguously anymore must be set aside and excluded from further use.

Sterilization method and parameters Each aneurysm clip in its unopened original packaging has been packed and sterilized individually and is supplied as a sterile product. An aneurysm clip must be regarded as unsterile e.g. if the sterile packaging is open, torn, perforated or damaged, or if the sterility of the product has expired (use-by date). Sterilization has to be carried out through a validated sterilization process. Using a non-validated sterilization process may result in the aneurysm clip being unsterile. Sterilize the aneurysm clip in the appropriate storage devices recommended by Aesculap for Aesculap Yasargil aneurysm clips. For further information on the appropriate storage devices recommended by Aesculap, please contact Aesculap or consult the special brochures for titanium and Phynox aneurysm clips. These brochures too can be ordered from your Aesculap sales representative. The aneurysm clips are supplied sterile. Sterilization of a clip that has been removed from its sterile package may be accomplished by the following the sterilization process outlined in this section. Any permanent aneurysm clip that has come in contact with a patient's blood or bodily fluid should not, under any circumstances, be cleaned, re-sterilized or in any other way prepared for use in another patient. Sterilization of the device may be accomplished by steam. Aesculap does not recommend the device be sterilized by "Flash" or chemical sterilization. Surgical instruments may also be placed within the Aesculap rigid sterilization container (sterile container) for processing under generally accepted hospital in-use conditions. The recommended sterilization parameters are as follows: Aesculap advises against sterilizing the device by flash sterilization or chemical sterilization. Sterilization may be accomplished by a standard prevacuum cycle in a steam autoclave.

To achieve a sterility assurance level of 10-6, Aesculap recommends the following parameters: Aesculap Orga Tray/Sterile container (perforated bottom) Minimum cycle parameters* Sterilization method Temperature Time Min. drying time Prevacuum 270 F 4 min 20 min *Aesculap has validated the above sterilization cycle and has the data on file. The validation was accomplished in an Aesculap sterile container cleared by FDA for the sterilization and storage of these products. Other sterilization cycles may also be suitable, however individuals or hospitals not using the recommended method are advised to validate any alternative method using appropriate laboratory techniques. Use an FDA cleared accessory to maintain sterility after processing, such as a wrap, pouch, etc. Storage Store the aneurysm clips: In their sterile packaging or In a compatible storage system recommended by Aesculap, kept in a dust-free area protected from chemical fumes and extreme air or temperature fluctuations. For further information on the appropriate storage devices recommended by Aesculap, please contact your local Aesculap sales representative or consult the Yasargil Aneurysm Clip Brochure. Distributor in the US/Contact in Canada for product information and complaints Aesculap, Inc. 3773 Corporate Parkway Center Valley, PA 18034 USA SOP-AIC-5000566 Ver. 03 07/15 TA011251-US