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1. Indication and adjustment

Indication and adjustment LG Remote Interface Manual de instru es 06 2015 SITRANS SIEMENS Safety Guidelines Warning notices must be observed to ensure personal safety as well as that of others and to protect the product and the connected equipment These warning notices are accompanied by a clarification of the level of caution to be observed Qualified Personnel This device system may only be set up and operated in conjunction with this manual Qualifie
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1. Marques déposées : Indications : - K

Auteur de la documentation Alexandre Colot K Team S A Ch de Vuasset CP 111 1028 Pr verenges Suisse email infoQhemisson com Url www hemisson com MARQUES D POS ES Philips Koninklijke Philips Electronics Corp Sysquake Calerga SA MPLAB Microchip SA LabVIEW National Instruments Corp MATLAB MathWorks Corp Webots Hemisson Cyberbotics S A INDICATIONS Le contenu de ce manuel est susceptible de changer sans pr avis ou
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2. CONTRAINDICATION for Whole Body Vibration

CONTRAINDICATION for Whole Body Vibration Machine Pregnancy Acute Thrombosis Serious Cardiovascular Disease Pacemaker and Implantable Cardioverter Defibrillator Recent Wounds from an Operation or Surgery Artificial Joints recent Recently Placed IUD s Metal Pins or Plates Acute Hernia Discopathy or Spondylosis Type Diabetes Epilepsy Vertigo and neurologic conditions that affect balance Severe Migraines Tumors cancerous Retinal Detachment Known Retinal Conditions H
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3. indications réactif protocole performance références - Sigma

SIGMA ALDRICH COLORANT DE WRIGHT Pour le Geometric Data Hemastainer et le Hematrak Protocole N WSGD 128 INDICATIONS La solution du colorant de Wright est destin e tre utilis e pour la coloration des frottis sanguins ou de moelle osseuse Les solutions sont destin es un usage diagnostique in vitro Le colorant de Wright r f rence N WSGD 128 est un colorant de Romanowsky modifi utilis pour colorer de mani re diff rentielle les divers l ment
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4. Patient handling device including local status indication, one

US 8 689 376 B2 Page 2 56 References Cited WO WO 01 85085 A2 11 2001 WO WO 2004 093023 A2 10 2004 U S PATENT DOCUMENTS OTHER PUBLICATIONS 4 882 566 A 11 1989 Koerber Sr et al 4 907 845 A 3 1990 Wood PCT Written Opinion of the International Searching Authority 4 998 939 A 3 1991 Potthast et al i 5 137 033 A 8 1992 Norton regarding PCT US06 043290 the international counterpart to the 5 195 198 A 3 1993 Travis present application that includes the same claims as the
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5. Indication and adjustment

Indication and adjustment LG Remote Interface Manual de instru es 06 2015 SITRANS SIEMENS Safety Guidelines Warning notices must be observed to ensure personal safety as well as that of others and to protect the product and the connected equipment These warning notices are accompanied by a clarification of the level of caution to be observed Qualified Personnel This device system may only be set up and operated in conjunction with this manual Qualifie
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6. Conditions de non contre-indication à la plongée sous

Conditions de non contre indication la plong e sous marine de loisir pour les sujets prenant un traitement m dicamenteux b ta bloquant Recommandations pour la FFESSM B BROUANT R KRAFFT V LAFAY B LEMMENS F ROCHE G FINET B GRANDJEAN Groupe de travail b ta bloquants et plong e de la Commission M dicale et de Pr vention de la F d ration Fran aise d Etudes et de Sports Sous Marins Propositions valid es par le Comit Directeur National de la FFESSM du 3
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7. Mises en garde, précautions et indications diverses Mise en route

Mise en route Feuille isolante Avertissement Accessoires fournis el la e Rangez la pile dans un endroit hors de port e des enfants Si un enfant avale accidentellement la pile Apr s avoir d ball l appareil elIecommande consultez imm diatement un m decin v rifiez que vous disposez de tous Lorsque vous utilisez la e Ne rechargez pas la pile ne la soumettez pas un court circuit ne la d montez pas ne la chauffez pas les l ments suivants t l commande
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8. contraindication for pneumatic compression

CONTRAINDICATION FOR PNEUMATIC COMPRESSION e Prone to bleeding or taking any blood thinners Prone to or bruises easily Surgical implants Pregnancy Acute Thrombosis Serious Cardiovascular Disease Pacemaker and Implantable Cardioverter Defibrillator Recent Wounds from an Operation or Surgery Artificial Joints Recently Placed IUD s Metal Pins or Plates Acute Hernia Discopathy or Spondylosis Type Diabetes Severe Migraines Tumors cancerous Pulmonary Emboli
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9. WIRELESS DOOR CHIME WITH VISUAL INDICATION DRAADLOZE

PEREL EDB7 WIRELESS DOOR CHIME WITH VISUAL INDICATION DRAADLOZE DEURBEL EN ONTVANGER MET VISUELE SONNETTE ET RECEPTEUR AVEC INDICATION VISUELLE TIMBRE Y PULSADOR INALAMBRICOS FUNK T RGLOCKE UND FUNK KLINGELTASTER BEZPRZEWODOWY DZWONEK DO DRZWI I GONG Z SYGNALIZACJIA WIZUALNA CAMPAINHA SEM FIOS COM INDICADOR VISUAL USER MANUAL 3 GEBRUIKERSHANDLEIDING 7 MODE D EMPLOI 11 MANUAL DEL USUARIO 15 BEDIENUNGSANLEITUNG 19 INSTRUKCJA OBSLUGI 24 MANUAL DO UTILIZADO
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10. H5i ClimateLine / ClimateLine Indications for use

RESMED a TM H5i HEATED HUMIDIFIER TM Climateline Climateline HEATED AIR TUBING MAX Information Guide English e Svenska e Dansk e Norsk e Suomi English Indications for use The H5i is indicated for the humidification of the air delivered from a CPAP or bilevel device The H5i is for use only as recommended by a physician The H5i is intended for single patient re use in the home environment and re use in a hospital i
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11. UT55A/52A Digital Indication controllers Operation Guide for Single

Operation UT55A UT52A UTAtivanced Digital Indicating Controllers i Guide Operation Guide for Single loop Control IM 05P01C31 11EN Installation and Wiring YOKOGAWA Yokogawa Electric Corporation 4th Edition Jan 2011 This operation guide describes installation wiring and other tasks required to make the controller ready for operation Contents Safety Precautions Model and Suffix Codes How to Install Hardware Specifications How to Connect Wires T
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12. Indications for use: Technical data: Ordering information: Precision

hydro Precision impression material silicone based condensation curing 1 Tray preparation Select a tray type suited for desired application For optimal adhesion of impress ion material we recommend use of sili Adhesive liquid or spray Apply a thin layer of adhesive film onto the tray and let dry for 60 seconds Fig 1 Take liminary impression with hydroC putty 2 Preliminary impression Fill measuring scoop evenly to top with hydroC putty Fig 2 Smooth hydr
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13. 3. product outlook 4. led indication 5. installing the

3 PRODUCT OUTLOOK Right View i Fiber TP TX RX O O ACT Ol T OO m a oo FDX PWR Gigabit Ethernet Converter 1000Base T to 1000Base SX LX Fiber TP ACT ac OOE I OO FDX PWR Gigabit Ethernet Converter 1000Base T to 1000Base SX Fiber TP WDM ACT cae MELA h d CC i OO FDX PWR Gigabit Ethernet C
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14. Control panel LED indications Applications

lt 6 AGATEG 1 ON button Press to cycle through AE a Level horizontal fan line b Plumb vertical fan line Checking the horizontal line front to back c Cross line horizontal and vertical 1 Set up the CL30 about 6 15 cm away from a wall d Locked cross line manual mode El Surface 1 and 12 15 ft 4 5m from another wall Surface 2 e Off 2 Turn it on in cross line mode Be sure it s self leveling 2 LED for laser mode low battery 3 Carefully mark the
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15. O-arm® Imaging System Supplemental Guide Indications for Use

O E Technical Support a gt Medtronic 800 595 9709 Toll Free 720 890 3160 Local and International O arm Imaging System Supplemental Guide Indications for Use The O arm Imaging System is a mobile X ray system designed for 2D fluoroscopic use and 3D imaging and is intended to be used where a physician benefits from 2D and 3D information of anatomic structures and objects with high X ray attenuation such as bony anatomy and metallic objects The O arm Imaging Syst
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16. CONTRAINDICATIONS for Whole Body Vibration

CONTRAINDICATIONS for Whole Body Vibration Machine Precautions If any of the items listed below apply to you be certain to consult with your physician before using Whole Body Vibration Machine e Pregnancy e Acute Thrombosis e Serious Cardiovascular Disease e Pacemaker and Implantable Cardioverter Defibrillator e Recent Wounds from an Operation or Surgery e Artificial Joints recent e Recently Placed IUD s Metal Pins or Plates e Acute Hernia Discopathy or Sp
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17. Guideline for Data Projector Indications Fourth Edition

Guideline for Data Projector Indications Fourth Edition Revised in July 2014 Projector Terminology Working Group Japan Business Machine and Information System Industries Association JBMIA Table of Contents Mis PUR OSC isis sac sete a aes acca ela ws eee et ce ca esac ea elec es teen 3 23 OCODE rera ann Aaaa ei encsaseecstueecaneccaseseccensccacevenescaewenaas sesenecteareseccansccstessssensecaccs 3 Se dication M thod ossia a E a aaa 3 3 1 Parts of the main unit in
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18. / Description du logiciel Mimics / Indications d`utilisation

Ce document contient les Instructions pour l utilisation de base du logiciel Mimics Mi E Des instructions d taill es sont disponibles dans le manuel d utilisation Medical Edition L anglais est la langue utilis e pour l interface du logiciel Mimics Instructions pour l utilisation du logiciel Description du logiciel Mimics Materialise s Interactive Medical Image Control System MIMICS est un logiciel qui sert visualiser et segmenter des images m dica
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19. French 1. Indication d`utilisation 2. Instruction d`utilisation et

French 1 Indication d utilisation Le syst me d implant DIO peut tre install par 1 intervention ou par 2 interventions L utilisateur peut choisir de l employer pour soutenir des proth ses qui aident r tablir la fonction masticatoire chez le patient ou il peut fabriquer partir du syst me d implant les proth ses qui sont adapt es aux implants d j install s dans les machoires sup rieure et inf rieure 2 Instruction d utilisation et Proc dures lt Pr
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20. instructions for use indications for use contraindications

ulthera cel system INSTRUCTIONS FOR USE INDICATIONS FOR USE The Cellfina System is intended for long term improvement in the appearance of cellulite in the buttocks and thigh areas of adult females as supported by clinical data demonstrating no significant reduction in treatment benefits up to 1 year of observation CAUTION Federal law restricts this device to use by or on the order of a physician CONTRAINDICATIONS The System should not be used on patients who have
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