8 Technical Specifications
Multi-Parameter Mobile CareGuide™ Oximeter 4100
SmO2 Range 10% - 85%
Resolution 1%
Measurement Rate 30 seconds
Accuracy 4 SmO2 units (%)
Drift None
pHm Range 6.90 – 7.50
Resolution 0.01 pHm units
Measurement Rate 30 seconds
Accuracy 0.05 pHm units
Drift None
Packaging System Packaging 1 Multi-Parameter Mobile CareGuide™ 4100 Sensor
1 Android display with CareGuide™ software
1 display charger
1 Micro-USB to Type A adapter (if required)
1 tub of 100 Sklar™ wipes
1 box of 80 CleanTex™ wipes
1 case of 12 Mobile CareGuide™ 4100 Disposables
Packaging for
Reorders 1 Multi-Parameter Mobile CareGuide™ 4100 Sensor
1 case of 12 Mobile CareGuide™ 4100 Disposables
Multi-Parameter
Mobile CareGuide
Sensor Size • 129 x 54 x 15 mm (5.1 x 2.1 x 0.6 inches)
Weight 168.3 g (5.9 oz)
Sensor Cable Length • 2.13 m (7 ft)
Attachment to Patient • Insert into Mobile CareGuide™ 4100 Disposable
• Clean with Sklar™ and CleanTex™ wipes between patients
Shelf Life 2 years post manufacturing date
Use Life 2 years post first use
Mobile CareGuide
Disposable Size • 178 x 143 x 14 mm (7.0 x 5.7 x 0.6 in)
• One size fits shoulder, calf, or thigh.
Weight 13.1 g (0.5 oz)
Material • Latex free
• Biocompatible adhesive
Attachment to patient • Adhesive placement on shoulder, calf or thigh
• Intact skin only
• Single Use per patient
Shelf Life 18 months post manufacturing date
Use Life 72 hours (single use patient)
Power input requirements Host provides through USB cable Voltage: 5.0V DC +0.2V
Current Max: 700 mA
Alarms Audiovisual Visual equipment technical inops only via CareGuide™ display or 3rd party display
Error Conditions See Troubleshooting above.
Product Classification Medical Device US: Class II Type BF device per section 870.2700 of 21 CFR and IEC 60601-1 3rd Edition v2005
Standards Electrical & Constructional Safety IEC 60601-1-1:2005 (includes former PEMS IEC 60601-1-4)
Electromagnetic Compatibility IEC 60601-1-2: 2001/2006 (Class B emissions)
Laser Safety Class 1 laser device per IEC 60825-1: Edition 2.0 (2007)
Enclosure PC/UABS ProCAST HT;
Impact, rough handling, mold stress relief per IEC 60601-1 3rd edition
Shipping & Packaging ISTA 1A
Risk Analysis/Risk Management ISO 14971
Usability IEC 60601-1-6
Biocompatibility Cytotoxicity: ISO 10993-5: v2009
Irritation and Sensitization: ISO 10993-10 v2010
Cleaning AAMI TIR 12:2010;
AAMI TIR 30:2003
Electromagnetic Emissions and Immunity This equipment has been tested and found to comply with the limits for medical devices to IEC 60601-1 3rd Edition v2005. This testing shows the device provides reasonable protection against harmful interference in a typical medical installation. However, there is no guarantee that interference will not occur in a particular installation. If this equipment does cause harmful interference to other devices or is negatively impacted by other devices, the user is encouraged to try to correct the interference by one or more of the following measures:
• Reorient or relocate the devices.
• Increase the separation between the devices.
• Connect the equipment to an outlet on a different circuit.
• Contact the Service Center.
Operating Conditions Temperature 0oC – 50oC (32oF-122oF)
Humidity 15-95% ATM non-condensing
Altitude -170 – 4572 m (-557 – 15000 ft)
Manufactured by:
Reflectance Medical, Inc. (RMI)
116 Flanders Road, Suite 1000
Westborough, MA 01581 USA
Voice: +1.508.366.4700
Fax: +1.508.366.4770
Email:
[email protected]Website: www.reflectancemedical.com
Technical Support:
Voice: +1.508.475.9366
Email: techsupport@reflecta