MyDiagnostick AF Screening Device
Product Code: N101282
- Easy to use - metallic handles at both ends record an ECG when gripped
- High quality Atrial Fibrillation detection - highly sensitive and specific Atrial Fibrillation detection algorithm
- Highly portable - can be used anywhere and at any time of day making it ideal at screening for silent AF
- Large memory - stores over 100 ECGs with stored ECG strips retrievable via USB connection
- 2 year warranty
MyDiagnostick Atrial Fibrilation (AF) Screening Device.
It is the shape of a stick with metallic handles (electrodes) at both ends that record an ECG when gripped. The recorded ECG is of a high quality and the AF detection algorithm is highly sensitive and specific.
MyDiagnostick is able to record and store over 100 ECGs and the ECG strips stored can be retrieved through a USB connection by the physician, enabling clinical confirmation and documentation of AF.
MyDiagnostick is perfect for use by general practitioners and pharmacists to detect AF in patients. The portability of MyDiagnostick means measurements can be performed outside of the doctor’s office for a longer period of time. It can be used at home, at the office or anywhere at any time during the day, meaning it can be used to screen for silent AF. MyDiagnostick is supplied with a 2 year warranty.
What's in the box?
- MyDiagnostick ECG Recorder with AF Detection
- Protective case
- USB Cable
Length 260 mm
Diameter 22 mm
Weight max. 180 g
Batteries 2x NiMH 1.2V 2000 mAh rechargeable (not replaceable)
Charge time (from depleted state) max. 12 hours
Battery longevity min. 500 recordings of 60-70 s at full charge
Computer connection USB 2.0
Full Speed Power consumption max. 300 mA (charging, via USB connector)
Safety type BF (EN 60601)
Temperature (operating) +1 oC to +40 oC
Temperature (non-operating) -10 oC to +50 oC
Relative humidity (operating) 10% to 90%
Barometric pressure normal atmospheric pressure ranges
Ingress protection IP24 (EN 60529)
ECG storage capacity 140 recordings of 60-70 s
AF detection method R–R interval dispersion during 60 seconds
AF detection sensitivity min. 90% (as a result of adjusted ROC in detection)
AF detection specificity min. 95%
Classification Class 2A (93/42/EEC)
RoHS Complies with RoHS 3 according to directive EU 2015/863
EMC Complies with the conditions according to - directive IEC 60601-2-1