Description: Packing List: Package List: ECG Machine×1 ECG Wire×1 Limp Clip×4 Chest Suction Ball×6 Thermal Printing Paper×1 Fuse×1 Power Cable×1 Description: ? Specifications: standard 12 leads synchronously?12 leads Input circuit Floating; Protection circuit against Defibrillator effect Input Impedance ≥50MΩ Input circuit current ≤0.0.05μA Record mode Automatic: 3CH×4+1R, 3CH×4, 3CHx2+2CHx3,3CHx2+2CHx3+1R,6CHX2; Manual: 3CH, 2CH, 3CH+1R, 2CH+1R; Rhythm: Any selectable. Filter EMG Filter: 25 Hz / 30 Hz / 40Hz/75 Hz / 100 Hz / 150Hz DFT Filter: 0.05 Hz/ 0.15 Hz AC Filter: 50 Hz / 60Hz CMRR >100dB Patient current leakage ＜10μA Input Circuit Current ＜0.05μA Frequency Response 0.05Hz~150Hz (-3dB) Sensitivity? 2.5mm/mV, 5 mm/mV, 10 mm/mV, 20 mm/mV Anti-baseline Drift Automatic Time constant ≥3.2s Noise level ＜15μVp-p Paper speed 12.5 mm/s, 25 mm/s, 50 mm/s Recording mode Thermal printing system Paper specification 110mmx20m?paper?roll LCD display 7”?graphic LCD Safety classification IEC60601-1 class I, type CF Power supply AC:?100~240V, 50/60Hz, 30VA~100VA ? DC: 14.8V/2200mAh, built-in lithium battery Fuse AC220V±10% ?2*Φ5×20mm,T2A/250V ?AC time lag ? ? AC110V±10% ?2*Φ5×20mm,T4A/250V ?AC time lag >? Package List: ECG Machine×1 ECG Wire×1 Limp Clip×4 Chest Suction Ball×6 Thermal Printing Paper×1 Fuse×1 ? Power Cable×1 FDA declaration : Statement：The sale of this item may be subject to regulation by the U.S. Food and Drug Administration and state and local regulatory agencies. If so, do not bid on this item unless you are an authorized purchaser. If the item is subject to FDA regulation, I will verify your status as an authorized purchaser of this item before shipping of the item. This item has been cleaned and treated according to the manufacturer's instructions. The Fingertip Pulse Oximeter is certified with the US FDA 510K No. K070371, the CE & TUV of Eureope and it is on the Australian Register of Therapeutic Goods(ARTG) with the code 136606. The Powered Surgical Instrument / Speed 808 System is certified with the US FDA 510(k) Number：K132989 The Powered Surgical Instrument / Hair Remove Device is certified with the US FDA 510(k) Number：K180353 The Powered Surgical Instrument / Hair Remove System is certified with the US FDA 510(k) Number：K141973 massager, vacuum, light induced heating / Slimming Treatment Device is certified with the US FDA 510(k) Number：K161892
Price: 395.09 USD
Location: Shen Zhen
End Time: 2025-01-16T15:18:50.000Z
Shipping Cost: 0 USD
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Item Specifics
Restocking Fee: No
Return shipping will be paid by: Buyer
All returns accepted: Returns Accepted
Item must be returned within: 30 Days
Refund will be given as: Money Back
LCD display: 7” graphic LCD
Input circuit current: ≤0.0.05μA
Input Impedance: ≥50MΩ
Input circuit: Floating; Protection circuit against Defibrillator effect
lead acquisition: synchronously 12 leads
Lead: standard 12 leads
MPN: Does Not Apply
Brand: Carejoy
