Pulse oximeter,handheld,cont,w/resp rate

Product Code : SCL-MAI-12306
GENERAL DESCRIPTION
Handheld, portable, rechargeable battery-powered pulse oximeter, for the non-invasive spot-checking or continuous monitoring of patient oxygen saturation (SpO2), pulse rate, and respiratory rate.

TECHNICAL SPECIFICATIONS
Measurement:
SpO2, pulse rate and respiratory rate monitor, with plethysmography waveform, for adults, children and neonates.
SpO2 detection includes the range: 70 - 100%.
SpO2 resolution: 1%.
SpO2 accuracy (in the range at least 70 - 100%): ± 2% (no motion, low perfusion), ± 3% (motion) for all patients (infants, children, adults).

?Accuracy in patients with dark skin pigmentation has been validated through clinical studies.

Pulse Rate detection range: 25 - 240 bpm.
Pulse Rate resolution: 1 bpm.
Pulse Rate accuracy: within ± 3 bpm (no motion, low perfusion), ± 5 bpm (motion) for all patients (infants, children, adults).

Respiratory rate range: 4 to 70 rpm.
Respiratory rate resolution: 1 rpm.
Respiratory rate accuracy (no motion, adults/paediatrics (> 2 years)): within ± 3 rpm A(RMS), ± 1 rpm mean error.
(Note: device is indicated for spot-checking or continuous monitoring of Respiration Rate from the photoplethysmogram (RRp) of adult and paediatric patients (> 2 years) during no motion conditions).

Display:
Data display update rate: every 1s.
Display with main parameters: % SpO2, plethysmographic waveform, pulse rate, respiratory rate, signal quality, status messages, battery state indication.

Features:
Suitable for detection in low perfusion conditions.
Design enables use in demanding environments, e.g. shock, vibration.
Audible and visual alarms for low saturation and high/low pulse rate, thresholds settable by user.
Variable pitch to indicate changes in oxygen saturation levels.
Audible and visual alarms for sensor error or disconnected, system errors, low battery.
Alarm override and temporary silencing function.
Internal data storage for patient trends and event log.
Capable of working with adult, paediatric and neonatal reusable probes.

Casing:
Enclosure protection IP22.
Case and reusable probe suitable for cleaning and disinfection.
Overall device and probe weight < 400 g.

Electrical characteristics:
Operated by rechargeable Li-ion battery power supply.
External AC battery charger, plug style and voltage as per local supply.
Charger protects against over-voltage and over-current line conditions and is certified to IEC 60601-1.
Protection against defibrillator discharges.
Suitable for operating by mains power and by battery.
Automatic switch between battery and mains powered modes.
The display shows which power source is in use.
Running time on battery ≥ 12 hours (24h at lowest screen brightness and beep tone turned off).

ENVIRONMENTAL CONDITIONS
Storage conditions (packaged): -20 to 60°C, 10 to 95% relative humidity, non-condensing.
Operating conditions: 0 to 40°C while battery is charging, 0 to 50°C while battery is not charging, 10 to 95% relative humidity, non-condensing.

SUPPLIED WITH
2 x universal reusable sensors (for adults or children ≥ 3kg)
1 x battery charger
1 x set user and maintenance manuals in English/French/Spanish at minimum. Other languages can be requested. If digital manuals will be provided, then a quick reference guide in English/French/Spanish languages which clearly indicates the URL to access complete manuals will be supplied with each device.
1 x list of all equipment and procedures required for routine maintenance in Operator’s Manual.
1 x list of all spares and accessories, with part numbers and contact details for part supply in Operator’s Manual.
1 x contact details of manufacturer, supplier and local service agent in Operator’s Manual.

COMPONENT OF A KIT
Yes

?WEIGHT & VOLUME (Packaged)
?Weight: 1.0kg
?Volume: 4.3dm³

?ESTIMATED LEAD TIME
?3 weeks
?
?MATERIAL SAFETY DATA SHEET INFORMATION (MSDS)?
?Li-Ion (Lithium-Ion) battery, UN 3481 Class 9, Packing Group II.?
?
?MARKET CLEARANCE AND DEVICE CLASSIFICATION
?CE certified under the EU MDD 93/42/EEC or MDR 2017/745/EEC as Class IIb device.
USA FDA (Class II).