Medical Test Equipment

ISO18193:2021- Cardiovascular implants and artificial organs — Cannulae for extracorporeal circulation ISO18193:2021-Annex C Test set-up for recirculation Figure C.1 — Circuit for recirculation testing of dual-lumen cannula using ink or particles. Figure C.2 — Vascular model of superior vena cava, right atrium, and inferior vena cava for testing dual-lumen cannulae recirculation

ISO/DIS 18193:2020- Cardiovascular implants and artificial organs — Cannulae for extracorporeal circulation ISO/DIS 18193:2020-Annex B Test set-up for kink resistance

ISO/DIS 18193:2020- Cardiovascular implants and artificial organs — Cannulae for extracorporeal circulation ISO/DIS 18193:2020-Figure A.11 — Female reference conical fitting for testing male 6 % (Luer) lock fittings for separation force and resistance to overriding Packaging

ISO/DIS 18193:2020- Cardiovascular implants and artificial organs — Cannulae for extracorporeal circulation ISO/DIS 18193:2020-Figure A.4 Reference steel female conical fitting Packaging

ISO 80601-2-12 Test conditions for acoustic tests -test lung Adjustable parameter Test condition For a ventilator intended to provide tidal volume VT ≥ 300 ml 300 ml ≥ VT ≥ 50 ml VT ≤ 50 ml Tidal volume, VTa 500 ml 150 ml 30 ml Set rate 10 breaths/min 20 breaths/min 30 breaths/min I:E ratio 1:2 1:2 1:2 BAP 10 hPa (10cmH2O) 10 hPa (10cmH2O) 10 hPa (10cmH2O) Linear resistance,Rb 5 hPa·(l/s) −1 ±10% 20hPa·(l/s)−1 ±10% 50hPa·(l/s)−1 ±10% Isothermal Compliance, Cb 50 ml·hPa −1 ±10

ISO 80369-20:2015 and ISO 18250-1:2018 Annex D Subatmospheric Pressure Air Leakage Tester with test result printing function Technical parameters ●According to standards: ISO80369-20-Annex D ●Pressure gauge range:0~-80kpa ●Pressure gauge accuracy: ±0.25%FS ●Test time: 0-9999s Can be set ●Test time: 0-9999s Can be set ●Control mode: PLC+7 inch touch screen ●Output and input pipe size: φ4mm ●Dimensions: 360*380*210 mm W * D *h ●Weight: 11.5kg ●Power supply: 220V 50HZ This

ECG electrode electrical performance tester This equipment is a specialized equipment for electrode integrated performance testing, designed under the Test Method of disposable ECG electrode ANSI/AAMI EC12:2000(R2005) Disposable ECG electrodes Test items Incentive conditions scope Accuracy Testing time Impedance Sinusoidal alternating curret 100μAp_p - 5% 10Hz±10% 0-20KΩ Less than or equal to 1KΩ 2%±10Ω>1KΩ 3% >60s Disorder DC input impedance Greater than or equal to 10μΩ

Cone Tool -medical beds for children, BS EN 50637:2017-Figure 201.102a It is designed according to the standard BS EN 50637:2017-Figure 201.102a​. It is made of Stainless steel and weighs 3.3 ± 0.05kg Model KP-06371 According to standard IBS EN 50637:2017-Figure 201.102a Total weight 3.3 ± 0.05kg Surface roughness 1.6μm Material Stainless steel

IS0 10651-4 Figure 1 32 mm plug and ring gauges ISO 10651-4 2023.pdf specifies dimensional and gauging requirements for cones and sockets intended for connecting anaesthetic and respiratory equipment, e.g. in breathing systems, anaesthetic gas scavenging systems, and vaporizers. The cones and sockets are therefore not regarded as devices in their own right. It gives requirements for the following cones and sockets: 8,5 mm and 11,5 mm sizes intended for use in neonatal and

Capacitor Discharge Tester Description For IEC Testing of residual voltage after plug disconnect. The KP-1060 disconnects the line at the voltage peak and analyzes results to the requirements of various Standards, allowing quick results. Scope output for viewing decay waveform. Presets for IEC 61010-1, IEC62368-1, IEC 60601-1 and IEC60335-1. Features Accurate; in accordance with CTL voltage and time specifications. Disconnects input test voltage at positive or negative peak,

Human body mass distribution for a 135 kg patient and body part -figure AA.1 of IEC 60601-2-46 Subclause 201 .9.4.2.2 – Instability excluding transport position Human bodies do not gain mass at the same rate in all body parts, thus IEC 60601 -1 :2005,Figure A.1 9, is not representative for morbidly obese PATIENTS . Figure AA.1 , in combination with Table AA.1 , is recommended for use for higher mass PATIENTS . Figure AA.1 represents a 135 kg "baseline" PATIENT mass. For SAFE

Dynamic forces due to loading from persons- IEC60601-Clause 9.8.3.3 1. According to IEC60601-2-52 Section 201.9.8.3.3.1 for dynamic loading force tests from human weight. According to IEC60601-2-52 Appendix CC.2.2 Impact test of mattress support table. According to IEC60601 section 9.4.2.3 Instability. According to IEC60601 section 9.8.3.3 human body test mass. 2 IEC60601 section 9.8.3.3 2.1) Extension mode: motor drive 2.2) Impact height: 0~300mm adjustable 2.3) Material of

ISO 20696 Apparatus for testing Sterile urethral catheters until kinking

ME Equipment Rough Handling Tester Comply with IEC60601-1,GB9706.1-2020 standard 9.4.2.4.2, 9.4.2.4.3, 15.3.5 chapter requirements Technical parameters: 1. Power supply: AC 220V 50/60HZ 2, driving mode: servo motor, horizontal drive, automatic simulation of human hands to push ME equipment to cross the threshold of motion and rough handling test. 3, Speed: 0.8m/s± 0.1m /s (speed 0-2m/s can be set) 4, pushing force range: 0-2000N, accuracy: ± 1% 5, count: 0~9999 times can be

IEC 60601-2-52 Medical beds side rail strength and latch reliability tester According to standard IEC 60601-2-52-cl.201.9.8.3.3.3 Through PLC program control, 7 inch touch screen display, the use of electric cylinder to apply the test required force value, through high-precision sensor automatic data acquisition, can be arbitrarily set the test load value, load application time, test force peak acceleration capture function, maintain force stability function, reach the set

ISO 80601-2-70 figure 21.101 standard resistance Key D is the internal diameter: (4 ± 0,1) mm L is the length: (40 ± 1) mm A is the angle (45 ± 1) ° Break all edges with 0,15 mm to 0,20 mm radius or 45° chamfer. Drawing is not to scale. Connector: 15/22mm standard connector can be made according to customer requirements

According to standard IEC 60601-1-8

ISO 5364 Figure C.1 Test method for patency of lumen According to the standard ISO 5364 -Annex C Technical parameters Technical indicatorsForce: 5N±0.5NSteel ball diameter: 1.875 mm, 2.25 mm and 2.625 mm, 3.0 mm, 3.375 mm and 4.125 mm

ISO 5364 Figure B.1 Apparatus for testing resistance to collapse of the buccal portion According to the standard ISO 5364 -Annex B Feature The weights are driven by pneumatic force. During the test, only the driving air source needs to be provided for operation, and no power is required. It will automatically stop when the force value is reached, and the force value is precise. Simple operation Technical parameters Axial force: 100N,200NPressing block Angle: 60°±2°The arc

Product Description: The Test Equipment product available in our store falls under the category of Diagnostic Equipment, specifically designed for conducting energy-related tests. With an energy range of 50-55 joules, this equipment is essential for accurately measuring and analyzing energy levels in various systems and components. One of the key features of this Test Equipment is its discharge resistor, which is set at 50Ω ±1%. This precise resistor ensures stable and