5010e_513.doc / 22.01.10
SYMBOLS
The packaging material, the type plate on the instrument and the manual may contain the following symbols or
abbreviations:
Manufactured by:
This product fulfills the requirements of Directive 98/79/EC on
in vitro diagnostic medical devices.
In vitro diagnostic medical device
Caution (refer to accompanying documents)!
Please refer to safety-related notes in the manual accompanying this device.
Please consult instructions for use
Symbol for the marking of important information for appropriate handling of the device
Description of the technical specifications according DIN 58 960 part 4
Biohazard
Samples containing material of human origin must be treated as potentially infectious.
The relevant laboratory guidelines on safe use must be observed.
Symbol for the marking of electrical and electronics devices according to § 7 ElektroG
IP XO
No special protection against penetrating moisture (IP = International Protection)
REF
Order number
SN
Serial number
INSTRUMENT APPROVALS
The Photometer 5010 meets the requirement stated in Directive 98/79/EC of the European Parliament and the
Council of the European Union (EU) on in vitro diagnostic medical devices. Furthermore, the Photometer 5010
is manufactured according to the special safety requirements for IVD medical devices stated in DIN EN 61010,
testified by TÜV Rheinland Group.
The Photometer 5010 fulfils the EMC immunity requirements for laboratory use equipment according to the
EMC standard EN 61326.
ROBERT RIELE GmbH & Co KG Page 2 GENERAL NOTES
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