ResMed VPAP S manual Vpap S Features Summary, Technical Specifications, Product Codes

VPAP S FEATURES SUMMARY

Modes of operation

•S (Spontaneous)

•CPAP (with EPR)

Product features

•Simplified standard setting menu

•Vsync automatic leak management

•TiControl (Ti max/min)

•Adjustable breath trigger/cycle

•24V DC input (via converter)

•Compact S8™ design

•Easy-Breathe motor

Heated humidification

• Optional, fully integrated

Data storage

•Usage and treatment summary (day, week, month, six-month, year)

•Usage profile

•Summary data storage

•Detailed data storage

•Remote settings adjustment

Data transfer

•Direct download to PC

•ResLink via SmartMedia card

•ResScan Data Card

•Live oximetry with ResLink

•Remote compliance monitoring via ResTraxx

TECHNICAL SPECIFICATIONS

Performance

Operating pressure range: 3 to 25 cm H2O

Maximum single fault pressure: 40 cm H2O

Dynamic pressure characteristics

S mode: IPAP: 4 to 25 cm H2O; EPAP: 3 to 25 cm H2O

CPAP mode: 4 to 20 cm H2O

Sound pressure level

<26 dB (tested in accordance with the requirements of ISO 17510-1:2002)

Data storage

Data includes usage, leak, pressure, AHI, AI, tidal volume, respiratory rate and minute ventilation

Via LCD menu: 365 sessions of summary data

Via ResLink: 365 sessions of summary data, 30 sessions of detailed data

Via ResScan Data Card: 180 sessions of summary data, two sessions of detailed data

Dimensions (L x W x H): 4.4” x 6.5” x 5.7” (112 mm x 164 mm x 145 mm)

Weight: 2.9 lb (1.3 kg)

Power supply

Input range 100–240VAC, 50–60Hz, 40VA (typical power consumption),

<100VA (maximum power consumption), 12–24DVC via ResMed DC 24V/50W converter

Environmental conditions

Operating temperature: 41°F to 97°F (+5°C to +35°C)

Operating humidity: 10–95% non-condensing

Electromagnetic compatibility

Product complies with all applicable electromagnetic compatibility requirements (EMC) for residential, commercial and light industry environments according to IEC 60601-1-2.

Air filter

Two-layered, powder-bonded, polyester non-woven fiber

IEC 60601-1 classification

Class II (double insulated), Type CF

Note: The manufacturer reserves the right to change these specifi cations without notice.

PRODUCT CODES

VPAP S		26119
H4i with standard water chamber		26940
VPAP S + H4i		26120
S8	ResLink	22206
Oximeter Kit		1430050
S8	ResTraxx US	22204
S8	ResTraxx Canada	22221

ResMed Corp Poway, CA, USA +1 858 746 2400 or 1 800 424 0737 (toll free), ResMed Ltd Bella Vista, NSW, Australia +61 (2) 8884 1000 or 1 800 658 189 (toll free). Offices in Austria, Belgium, Brazil, China, Finland, France, Germany, Greece, Hong Kong, India, Ireland, Italy, Japan, Malaysia, Mexico, Netherlands, New Zealand, Norway, Portugal, Singapore, South Africa, Spain, Sweden, Switzerland, United Kingdom (see website for details). EPR, HumidAire, ResLink, S8, ResScan, ResTraxx, TiControl, and Vsync are trademarks of ResMed Ltd. H4i and VPAP are trademarks of ResMed Ltd and are registered in U.S. Patent and Trademark Office. ©2008 ResMed. 1011085/1 08 10

Global leaders in sleep and respiratory medicine www.resmed.com