-40%
FDA Fetal Heart Rate Detector Pregnant Pocket Fetal Doppler Baby Heart Monitor
€ 15.83
- Description
- Size Guide
Description
Description:Instructions:
Pocket Fetal Doppler is a hand-held obstetrical unit, which can be used in hospital, clinic and home for daily self-check by pregnant woman.
The fetal doppler is equipped with a full high definition color LCD display.
Features:
Beautiful shape,portable,easy operation
Easy-to-use,the probe can be changed
Accurate FHR detection with clear sound
High sensitivity interchangeable probe
Battery status indicator
2 display Interface : Digital display interface, Curve display interface
10 set default user data storage function.
High accuracy, curve display interface, can see the fetal movement curve.
Specification:
Standard: EN61266:1995
Safety Classification: BF
/Class
Ⅱ
/Internal power
Overall Sensitivity:
≥
90 dB (Integrated sensitivity 200mm away from the surface of the probe)
Measuring integrated sensitivity
The Doppler frequency :(300 ± 50) Hz
Reflecting target speed:10cm / s ~40cm / s
Ultrasound transducer’s effective area: 6.0±0.5cm2.
Target velocity and display range : No narrower than 50bpm-240bpm (± 2bpm). (Beat Per Minute)
(Notes: Please go to see a doctor once the FHR is abnormal) Output power:
≤
10Mw/cm2
EMC testing data (See annex
Ⅱ
)
Working frequency:3.0 MHz
±
10%
Spatial-peak temp-peak acoustic pressure:
≤
0.1 MPa. Effective area of transducer:6.0
±
0.5 cm2
Physical Characteristic:
Working environment: Temperature: +5
℃
~ +40
℃
Humidity:
≤
80% Atmospheric pressure: 86kPa ~ 106kPa
Transport and storage environment:
Atmospheric pressure: 86kPa ~ 106kPa,well-ventilated room without corrosive gases.
Battery: Two pieces of 1.5V battery(not include)
Size: 135mm (Length) ×65mm (Width) ×30 (Height) mm
Weight: 176g(without batteries)
Probe:
Working Frequency:3.0MHz
P-:
≤
1MPa
Iob
≤
20mW/cm2
Ispta
≤
100mW/cm2
Packing Include:
1 x Color LCD Fetal Doppler
1 x English user's manual
Am 28.09.20 hat der Verkäufer die folgenden Angaben hinzugefügt:
The following FDA Discl
aimer is required for
all eBay listing in Healthcare category and is included for REFERENCE:
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, We
will verify your status as an authorized purchaser of this item before shipping of the item.
(Seller Name: Tina Liu;Country: China;City: Beijing;TEL.:86-18838974545).
CE Certificate
The Fingertip Pulse-Oximeter is registered on the Australian Register of Therapeutic Goods (ARTG) with the code 136606, and certified by FDA of United States (Premarket Submission Number (510K): K073454 Listing Number: D045684, K082641 Listing Number: D064765, K090671 Listing Number: D078664); and CE Approved, TUV of Europe (Cert.No. : G1 10 02 50972 013). You can consult with the FDA's Center for Devices and Radiological Health.