Symbol Identifi Cation - arjo HUNTLEIGH DMX Mode D'emploi

EN
4.2 Symbol Identifi cation
Patient applied parts (ultrasound probes, PPG sensors and cuff s) are type BF according to the
defi nitions in IEC 60601-1.
General Warning
This symbol signifi es that this product, including its accessories and consumables is subject to
the WEEE (Waste Electrical and Electronic Equipment) regulations and should be disposed of
responsibly in accordance with local procedures.
This symbol signifies that this product complies with the essential requirements of the Medical
Device Directive (93/42/EEC) - Medical Device Regulation (EU/2017/745).
RxOnly
Federal law restricts this device to sale by, or on the order of a licensed healthcare practitioner.
Made in
Huntleigh Healthcare Ltd.
in the UK
35 Portmanmoor Road, Cardiff, CF24 5HN, United Kingdom
by:
T: +44 (0)29 20485885 sales@huntleigh-diagnostics.co.uk
www.huntleigh-diagnostics.com
Legal Manufacturer in association with the CE mark in Europe
ArjoHuntleigh AB
Hans Michelsensgatan 10 211 20 Malmö, Sweden
IP20
Protected against ingress of solid foreign objects >12.5 mm diameter.
Not protected against ingress of water.
IPx1
Protected against vertically falling water drops.
Power On/Standby
DI
Device Identifi er
REF
Reference Number
Fragile
Atmospheric Pressure Limitations
Temperature Limitations
LATEX FREE
LATEX
Does not contain Latex
Headphone Socket
Volume Up
Note: Product labelling should be readable from a distance of up to 0.7m.
Attention, consult accompanying
documents / Instructions for Use
USB Port
SN
Serial Number
MD
Medical Device
Keep Dry
Relative Humidity Limitations
Cardboard packaging can be recycled
PVC FREE
PVC
Does not contain PVC
Alignment mark
Volume Down