TECHNICAL SPECIFICATIONS
CardiAid CT0207RS/CT0207RF
Defibrillation System | |
Operating Mode: | Automated (CT0207RS: one button operation, CT0207RF, full-automatic). |
Wave Form: | Biphasic, current based. |
Energy delivery: | Adjusted to patient impedance, programmable (factory settings). |
Delivered energy – Adult mode: | 170j (Average for 50 Ω at low level energy), 270j (Average for 50 Ω at high level energy). |
Delivered energy – Paeditric mode: | 50j (Average for 50 Ω at low level energy), 75j (Average for 50 Ω at high level energy). |
Shock Sequence: | Constant or escalating, Programmable (factory settings). |
Charging Time: | Typically < 10 seconds*, maximum < 15 seconds.* |
ECG Analysis system | |
Analysis Time: | Typically <10 seconds.* |
Derivation: | II |
Asystole Threshole: | <0,160 mV |
Specificity NSR/ Asustolie: | >95** |
Sensitivity VF / pVT: | >90** |
Reaction to implanted Pacemaker: | Normal cardiac pacemaker rhythms are not detected as shockable. |
Movement detection: | Checks signal quality, gives acoustic warning at patient movement. |
Operation | |
Operating Elements: | i) Automatic switch-on when the cover is opened. ii) Flashing shock button (one-button operation for CT0207RS, full-automatic operation for CT0207RF). iii) Info-button. |
Info Mode | Announcement of the elapsed time and number of shocks since device started, when info-button is pressed. |
Display Elements: | Self-explanatory illuminated symbols (traffic light principle). Device status symbols (for self-test result). |
Defibrillation Electrodes | |
Range of Application: | Adult electrodes for patients :8 years / 25 kg. Paediatric electrodes for patients 1-8 years / <25 kg. |
Delivery status: | Disposable, self-adhesive, single-use electrodes; ready-to-use, sealed and packed with connector outside pouch. |
Polarization: | Not polarized (Exchange acceptable). |
Active Surface Area: | 200cm2 (adult), 80cm2 (paediatric) |
Cable length: | 130 cm |
Shelf Life: |
Adult and paediatric: 36 months from the manufacturing date |
Data Management | |
Event Documentation: | Automatic recording of ECG and event data in internal memory up to 4 sessions with a total maximum duration of 2 hours 50 minutes. |
Data Transfer: | Bluetooth (only for authorized service providers). |
Event Review and Device Programming: | Via bluetooth connection to PC with Cardiaid Monitor Software (only for authorized service providers). |
Self-test | |
Schedule: | Automatic; daily, monthly and when device is opened. |
Timing: | Programmable (factory setting) |
Scope: | Battery, electronics, software, charging. |
Energy Source* | |
Type: | Alkaline |
Capacity: | Up to 210 shocks. |
Monitoring Capacity: | Up to 20 hours |
Stand-by period: | 42 months |
Environmental Conditions | |
Operation: | i) Temperature: 0˚C to 50˚C ii) Humidity: 0-95% iii) Air Pressure: 572-1060h/PA |
Storage and Transport: | i) Temperature: 0˚C to 50˚C ii) Temperature: -20˚C to +70˚C (max. 2 weeks, without battery & electrodes) ii) Humidity: 0-95% iii) Air Pressure: 500-1060h/PA |
Standards | |
Device Class: | III |
Resuscitation Protocol: | ERC, ILCOR 2020 |
Norms: | IEC 60601-2-4: 2011+A1:2019 |
EMC: | EN 60601-1-2: 2015+A1:2020 |
Free Drop: | IEC 60601-1: 2006 + A1: 2013+AC:2014+A12:2014+A2:2020 |
Protection Class: | EN 60529:1992+A2:2016 (Dust protected, protected against water jets) |
Dimensions and Weight* | |
Dimensions: | 301 x 304 x 112mm |
Weight: | 3,0 kg (including battery and electrodes) |
* measured with a new battery pack, 20˚C. Values can vary within a non-significant tolerance and are dependent upon storage and environmental conditions, frequency of use, pre-configured settings and the shelf life of the product.
** The algorithm and the board of CardiAid CT0207 AED offer the optimum combination of sensitivity and specificity. (Published in “Automated analysis of electrical signals of the human body for detecting of life threatening cardiac abnormalities”, Igor Tchoudovski, Mensch and Buch Verlag, ISBN 3-89820-984-9, Pg 141)
Cardia International, at its own discretion, reserves the right to make changes pertaining to the technical features and the accessories of the device.
Cardia International, under no condition, shall be liable for any fault of spelling and/or writing in any and all instructive and informational data, documents, images given above and any direct, indirect, accidental, secondary legal or penal loss or damages may arise from them.