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HIGH SENSITIVITY

POCKET DOPPLERS

FD1/FD2/FD3

Содержание FD1

Страница 1: ...HIGH SENSITIVITY POCKET DOPPLERS FD1 FD2 FD3...

Страница 2: ...bstetric Mode 10 3 3 After Use 12 4 Care and Cleaning 13 4 1 General Care 13 4 2 General Cleaning and Disinfecting 14 4 3 Cleaning and Disinfecting Patient Applied Parts 14 4 4 Maintenance and Repair...

Страница 3: ...ein VP8HS EZ8 7 Posterior Tibial Vein VP8HS VP10HS EZ8 8 Posterior Tibial Artery VP8HS EZ8 9 Vertebral Artery VP4HS VP5HS 10 Carotid Artery VP5HS VP8HS EZ8 11 Subclavian Artery VP4HS VP5HS 12 Brachial...

Страница 4: ...e Instructions for Use to hand for future reference Attention consult this manual Refer to safety section Attention consult accompanying documents Instructions for Use 1 1 Warnings Do not use in the p...

Страница 5: ...e is identified and eliminated Any equipment connected to RS232 interface must be compliant with IEC60601 1 2005 Connect headphones only to the headphone socket Dopplex Dopplers are screening tools to...

Страница 6: ...ately the unit is received Should any damage be evident or any parts missing ensure that Huntleigh or your distributor is informed at once Storage Should the unit not be required for immediate use it...

Страница 7: ...Port 3 LCD Panel 4 Loud speaker 5 On Off Button 6 Probe Holder 7 Volume Control 8 Start Stop Button 9 Mode Button 10 Battery Compartment 11 Pocket Clip 8 9 10 11 7 2 4 Product Labelling Patient applie...

Страница 8: ...Portmanmoor Road Cardiff CF24 5HN United Kingdom T 44 0 29 20485885 sales huntleigh diagnostics co uk www huntleigh diagnostics com Legal Manufacturer in association with the CE mark in Europe ArjoHun...

Страница 9: ...for vascular examinations VP4HS 4MHz 1 for deep lying vessels VP5HS 5MHz 1 for deep lying vessels and oedematous limbs VP8HS 8MHz 1 for peripheral vessels VP10HS 10MHz 1 for specialist superficial ap...

Страница 10: ...and must not be immersed Clinical Use Apply a liberal amount of gel to the abdomen Place the faceplate of the probe flat against the abdomen above the symphysis pubis Adjust the probe to obtain an op...

Страница 11: ...ress and hold Start Stop button and immediately count the audible heart beats counting the first beat as the button is pressed The LCD displays the flashing clock symbol and the FHR reading is shown a...

Страница 12: ...button If you forget to switch the unit off it will automatically shut off after 3 minutes 2 Refer to the cleaning section before storing or using the unit on another patient 3 Store unit together wi...

Страница 13: ...k with your facility s local infection control policy and medical equipment cleaning procedures Observe warnings and guidance on cleaning fluid labelling regarding use and personal protective equipmen...

Страница 14: ...isk as defined below Risk Definitions Procedure Low Normal use or low risk situations include patients having intact skin and no known infection 1 Remove soiling wipe with a mild neutral detergent and...

Страница 15: ...the responsibility of the user for their efficacy and compatibility with the device 4 4 Maintenance and Repair Inspection is recommended each time the product is used paying particular attention to t...

Страница 16: ...Degree of safety of application in the presence of a flammable anaesthetic Equipment not suitable for use in the presence of a FLAMMABLE ANAESTHETIC MIXTURE WITH AIR OXYGEN OR NITROUS OXIDE 5 2 Stand...

Страница 17: ...e 9Vdc RS232 Interface FD2 only Data format RS232C Connector 8pin subminiature DIN socket Max applied voltage 5Vdc Battery Type IEC 6LR61 or IEC 6LP3146 Battery Life Typically 250 x 1 minute examinati...

Страница 18: ...sposal This symbol signifies that this product including its accessories and consumables is subject to the WEEE Waste Electrical and Electronic Equipment regulations and should be disposed of responsi...

Страница 19: ...aned to the outside of the package Mark the package Service Department FD1 FD2 FD3 For further details refer to NHS document HSG 93 26 UK only Huntleigh Healthcare Ltd reserve the right to return prod...

Страница 20: ...his medical device affecting the user or the patient then the user or patient should report the serious incident to the medical device manufacturer or the distributor In the European Union the user sh...

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