Indications for use System requirements Compatible ResMed ...

• Android™ 5.0 and later. Compatible ResMed devices • AirSense 11 • AirSense 10 • AirCurve 10. Note: Bluetooth features are only available on AirSense 11. Security : Built-in security features, steps you take to protect your smart device against malware, and keeping

  Devices, Android, Compatible

User guide - document.resmed.com

Use only ResMed parts (eg, air inlet filter, power supplies), masks and accessories with the machine. Non ResMed parts may reduce the effectiveness of the treatment, may result in excess carbon dioxide rebreathing and/or damage the machine. For compatibility information, refer to ResMed.com for more information. When using the humidifier tub:

  Resmed

AirFit F30i - Fitting guide - ResMed

Title: AirFit F30i - Fitting guide Created Date: 8/13/2019 10:03:58 PM

  Created, Resmed, F30i

Sleep Lab Titration Guide - ResMed

Female patients with mild to moderate OSA weighing more than weighing more than 66 lb (30 kg) 4–20 cm H 2O AutoSet/APAP (automatic positive airway pressure) Automatically adjusts pressure in response to flow limitation, snore and obstructive apneas OSA Patients weighing more than 66 lb (30 kg) 4–20 cm H 2O VAuto Automatically adjusts ...

  Guide, Patients, Mild

Travel Compliance Letter for ResMed Therapy Devices

Page 3 of 4 ResMed Corp 9001 Spectrum Center Blvd. San Diego, CA 92123 USA T 1 800 424 0737 F 1 858 836 5000 ResMed Pty Ltd 1 Elizabeth Macarthur Drive Bella Vista NSW 2153 Australia T +61 (2) 8884 1000 F +61 (2) 8884 2000 ResMed (UK) Ltd 8 Wimpole Street, London W1G 9SP, UK T +44 (1235) 862 997 F +44 (1235) 831 336 ResMed.com ...

  Letter

User guide - ResMed

The AirSense 10 CPAP device is indicated for the treatment of obstructive sleep apnea (OSA) in patients weighing more than 66 lb (30 kg). It is intended for home and hospital use. The humidifier is intended for single patient use in the home environment and re. use in a - hospital/institutional environment. Contraindications

  Obstructive, Sleep, Aaenp, Resmed, Obstructive sleep apnea, Airsense 10, Airsense

Home Oxygen Qualifying Guidelines - ResMed

The qualifying blood gas study/oxygen saturation test was performed by a physician, qualified provider or supplier of laboratory services that is registered and able to bill for the test, and the necessity for such testing must be documented in the patient’s medical record. C. All three qualifying exercise tests should be performed during the ...

  Qualifying

User guide - ResMed

• The Astral device may be used in the vicinity of electronic article surveillance (EAS) systems during mobile situations when attached to th e patient or patient’s wheelchair. The Astral device may experience interference in the vicinity of EAS. Keep the Astral device at least 8” (20 cm) away from the EAS.

  Guide, Surveillance, Electronic, Article, Astral, Electronic article surveillance

User guide - ResMed

When Pressure Relief is enabled, you may find it easier to breathe out. This can help you get used to therapy. SmartStart* When SmartStart is enabled, therapy starts automatically when you breathe into your mask. When you remove your mask, it stops automatically after a

  Easier, Breathe, Resmed

S9 Series AutoSet & Elite - ResMed

• Do not wash the air tubing in a washing machine or dishwasher. Weekly: 1. Remove the air tubing from the S9 device and the mask. 2. Wash the air tubing in warm water using mild detergent. 3. Rinse thoroughly, hang, and allow to dry. 4. Before next use, reconnect the air tubing to the air outlet and mask. Monthly: 1.

  Machine, Washing, Washing machine, Resmed

線量管理 「装置から提供される情報」

IEC60601-2-43 IEC60601-2-54 （計画中） 基準空気カーマ （面積線量， 入射表面線量） DICOM Dose SR Sup 94 ，CP-1223 IEC 61910-1 ed.1 (2014-09-24発行 ) CR/DR IEC60601-2-54 （計画中） Exposure Index （面積線量， 入射表面線量） DICOM Dose SR CP-1077 IEC62494-1 乳房用 X線装置 IEC60601-2-45 （計画 ...

  Iec60601, Iec60601 2

心電計 ECG-2150 - nihonkohden.co.jp

2） 本装置に接続する非医用電気機器は「、患者環境外（iec60601-1： 2005またはiec60601-1-1：2000）」に設置してください。患者環 境に設置すると、患者（被検者）および操作者が電撃を受けること があります。やむを得ず、患者環境に設置するときは、接続する機

  2015, Iec60601, Ecg 2150

Tobii Dynavox I-Series User’s Manual

IEC60601–1 China RoHS compliance. RoHS directive compliance. 1.3 Intended Use The Tobii Dynavox I-Series is an Augmentative and Alternative Communication (AAC) product, a purpose-built Speech Generating Device (SGD) designed to provide to its users increased communication ability and greater independence.

  Iec60601

Electrical Safety Analyzer - Fluke Biomedical

The integrated ANSI/AAMI ES1 and IEC60601-1 patient loads are easily selectable. The Product does these tests: • Line (Mains) voltage • Ground Wire (Protective Earth) resistance • Equipment current • Insulation resistance • Ground (Earth) leakage • Chassis (Enclosure) leakage • Lead to Ground (Patient) and Lead to Lead (Patient

  Iec60601

【仕 様】 - tokso.net

2 流量と圧力の調節が独立 状況に合わせて 多く～少なく、強く～弱く 吸引できます。 point 3 優しく幅広くたん吸引 少ない流量でゆっくり吸引しますので、本人に優しく安心です。 また、すぐに吸引する時は大流量で幅広くたん吸引ができます。 低高1

Edition 4.0 2014-02 INTERNATIONAL STANDARD NORME ...

IEC 60601-1-2 Edition 4.0 2014-02 INTERNATIONAL STANDARD NORME INTERNATIONALE Medical electrical equipment – Part 1-2: General requirements for basic safety and essential performance – Collateral Standard: Electromagnetic disturbances – Requirements and tests ...

  60601, Iec 60601

IEC 60601-1-2

Figure A.6 – Voltage induced in a 1-turn, 2 cm radius coil by a 2 cm radiating coil operating at 13,56MHz and H0 of 7,5 A/m (r.m.s.) ..... 68 Figure E.1 – Test plan development flow when SPECIAL ENVIRONMENTS are known..... 78 Figure E.2 – Sub-process for determination of

  60601, Iec 60601