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CMS 50DL Pulse oximeter – red LED display

R500.00 R500.00

Fingertip pulse oximeter for Oxygen saturation monitoring.

Out of stock

SKU: 494 Category:

Description

Features for Pulse Oximeter:

– Measure SpO2 and PR accurately
– LED display for SpO2 value and PR value, bargraph display
– Low battery voltage indicator
– Automatic power off when signal is not available for 4 seconds
– 2 AAA batteries support 30 hours continuously
– Mini size, light weight, convenient to carry
– Widely used in hospital, home healthcare, oxygen bar, community medical centre, alpine area, sports healthcare etc. Measure SpO2 and PR accurately

Specification for Pulse Oximeter:

Display LED display
SpO2 Measurement range: 35‹«?99%
Resolution: ±1%Accuracy: ±2% (70%‹«?99%), unspecified (<70%)
Pulse rate Measurement range: 30‹«?255 bpm
Resolution: ±1%
Accuracy: ±2bpm or ±2% (select larger)
Power 1.5V (AAA size)
alkaline battery x 2
Supply voltage: 2.6~3.6V
Working current ≤30mA
Interference resistance against ambient light Deviation between SpO2 in nature indoor lighting condition and in dark room is less than ±1%
Dimension & Weight 57 (L) × 31(W) × 32(H) mm
50g (with batteries)

 

Package Content:
– 1 x Fingertip Oximeter
– 1 x Lanyard
– 1 x English user’s manual
– 1 x Pouch

 

The Fingertip Pulse Oximeter is certified with the US FDA 510K No. K070374, the CE & TUV of Eureope and it is on the Australian Register of Therapeutic Goods (ARTG) with the code 136616.

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: www.fda.gov/cdrh/devadvice/; www.fda.gov/cdrh/industry/support/index.html; Phone number: 800.638.2041;

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