Visomat Pulsoximeter PO50 Handleiding

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EN-11EN-10EN-9EN-8

Pulsoximeter PO50

Instructions for Use

Pulsoximeter PO50

UEBE Medical GmbH

Bgm.-Kuhn-Str. 

 Külsheim, Germany

[email protected], www.uebe.com

Subject to technical modifications.

Reprinting, including of extracts, is prohibited.

© Copyright  UEBE Medical GmbH

PZN-

28020

   DA - EN



Technical informationElectromagnetic compatibility (EMC)

Guidance and manufacturer’s declaration - electromagnetic immunityThe device has been manufactured and tested with great care. However, in the

unlikely event of a defect being detected after delivery, we provide warranty in

accordance with the following terms and conditions:

During the warranty period of  years from the date of purchase we reserve the

right either to repair any such defect at our expense or to supply a perfect replace-

ment unit.

Excluded from the warranty are parts subject to normal wear and tear as well as

damage caused by non-compliance with the instructions for use, improper han-

dling (e.g. unsuitable power sources, breakages, leaking batteries) and/or disas-

sembly of the unit by the purchaser. Furthermore, no claims for damages against

us are substantiated by the warranty.

UEBE Medical GmbH

Service-Center

Zum Läger 

 Külsheim, Germany

Shenzhen IMDK Medical Technology CO., Ltd

, F, Guangming Tianan Cloud Park Building,

 Zhenmei Road, Zhenmei Community, Hinhu Street,

Guangming District,  Shenzhen, PRC

MedNet EC-REP GmbH

Borkstraße ,  Münster, Germany

Warranty claims can only be advanced in the warranty period and by presenting

proof of purchase. In the event of a warranty claim, the unit must be sent to the

following address together with the proof of purchase and a description of the

complaint:

The cost of returning the device to our factory shall be borne by the sender. Com-

plaints that are sent back without prepayment will not be accepted.

The statutory claims and rights of the buyer against the seller (for example, defect

claims, producer liability) are not restricted by this warranty.

Please note: In the case of a warranty claim, please make sure to enclose the proof

of purchase.

Warranty

Measuring range (SpO2): % -  %

Accuracy (SpO2):±  % at the level of  % -  %, unspecified

(<  %)

Measuring range (pulse rate) (PR):-

Accuracy (pulse rate) (PR):±  beats/minute

Power supply: x .V AAA batteries

Current: ≤  mA

Battery life:  AAA .V alkaline batteries

can be used continuously for  hours.

Low battery indicator

appears before the battery power becomes

too low.

Operating conditions:Ambient temperature  to  °C, rel. air

humidity  % to  %, air pressure  hPa

to  hPa

Storage and transport conditions:Ambient temperature - to  °C, rel. air

humidity  % to  %

Classification:Internal power supply by battery

Degree of protection against

electric shock:

Type BF

IP code:IP : Protected against solid foreign parti-

cles with a diameter of more than .mm,

protection against water droplets

Operating mode:Continuous operation

Expected service life: years

Size: x  x  mm

Scope of delivery:Pulse oximeter, instruction manual, batter-

ies, retaining strap

The device is intended for use in the electromagnetic environment specified

below. The customer or the user of the device should assure that it is used in

such an environment.

Emissions testComplianceElectromagnetic environment - guidance

RF emissions

CISPR 

Group The device uses RF energy only for its internal

function. Therefore, its RF emissions are very low

and are not likely to cause any interference in

nearby electronic equipment.

RF emissions

CISPR 

Class BThe equipment is suitable for use in Home

Health Environments and Professional Health

Care Environments limited to patient rooms and

respiratory treatment facilities in hospital or

clinics. The more restrictive acceptance limits of

Group  Class B (CISPR ) have been considered

and applied. The equipment is suitable for use

in the mentioned environments when directly

connected to the Public Mains Network.

Consult the instructions for use

Degree of protection against electric shock Type BF

Temperature limitation

Humidity limitation

Atmospheric pressure limitation

Authorised representative in the European Uniion

Importer

Unique Device Identification

Model number

Date of manufacture

Reference number = item number

Batch code

Medical device

Protected against solid foreign particles with a diameter of more than

.mm, protection against water droplets

Manufacturer

Caution

This product complies with Regulation (EU) / of the European

Parliament and Council dated  April  regarding medical products

and bears the mark CE  (TÜV SÜD Product Service GmbH).

Explanation of symbols

0123

IP22

Product specificaties