Name: Aitecs 2016 Perfusor Spritzenpumpe Syringe Pump
Brand: Aitecs 2016
SKU: 4 779027 250205
Price: 499.0 EUR
Availability: InStock

Moog-Aitecs 2016 Perfusor Spritzenpumpe Syringe Pump

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Moog-Aitecs 2016 Perfusor Spritzenpumpe Syringe Pump

Product Details

UPC-Strichcode: 4 779027 250205

Marke: Aitecs 2016

Weight: 2.30 kg

Advanced syringe pump. The moog-aitecs® 2016 is equipped with automatic syringe plunger capturing. The aitecs® 2016 offers enhanced safety, reliability, ease of use and flexibility. The aitecs® 2016 is extremely versatile and meets the needs of all patient types from neonatal to adults. The pump can be used as a standalone device or as part of a patient data management system (PDMS), clinical information systems (CIS) and infusion monitoring system (AIMS16). The pump has customized drug library (up to 350 drugs labels) and the event log, which is able to record more than 2,000 events. Graphic LCD display. Advanced communication (USB, IrDA interfaces). It is recommended to use the pump in anesthesiology and intensive care departments.

Items supplied with pump

1. The pump

2. Mounting clamp

3. Operator‘s manual

4. AC power cord

5. Packaging

In accordance with the international standard, IEC/EN 60601-1

Medical Electrical Equipment – Part 1: General Requirements for Safety, the pump is classified as:

• Class II

• Defibrillation-proof type CF applied part

• IP43 (ingress protection)

• Not suitable for use with flammable anesthetic mixtures with air, oxygen or nitrous oxide

• Continuous operation

CE123 This symbol represents compliance with the essential requirements according to Council Directive 93/42/EEC (14 June 1993) amended by 2007/47/EEC of the European Communities concerning medical devices.

The pump is classified of Class IIb as per European Council Medical Devices Directive 93/42/EEC Annex IX Rule 11.

Compliance

The pumps comply with IEC/EN 60601-1, IEC/EN 60601-1-2, IEC/EN 60601-1-6, IEC/EN 60601-1-8, IEC/EN 60601-2-24.

The pumps have been manufactured by the company, which has implemented and maintains a Quality Assurance System meeting the requirements of the standard ISO 13485. The pump complies with the valid revisions of stated standards at the time of the device release.