Regulatory Information; Labeling Information - MORIA One Use-Plus Benutzerhandbuch

3 REGULATORY INFORMATION

Customer Service Information
EUROPE
USA
Electrical Safety Standard

4 LABELING INFORMATION

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NON
STERILE
4
MORIA #65040-F-02.2017
MORIA S.A.
15, rue Georges Besse - 92160 Antony - France
Phone +33 (0) 146 744 674
Fax +33 (0) 146 744 670
moria@moria-int.com
http://www.moria-surgical.com
Contact your local dealer or MORIA
0459
Product registered at the Food and Drug Administration (FDA): 510(k) K040297
Caution USA only: Federal law restricts the use of this device to physicians or
licensed practitioners.
IEC 60601
For EU customers only: this symbol indicates that within the European Union,
the product must be discarded in a separate collection bin at the end of its useful
life. This applies not only to this device, but also all accessories, including the
footpedal and electrical motors, regardless of whether those accessories are
marked with the symbol. Do not dispose as unsorted municipal waste.
For users out of European Union: please refer to local environmental regulatory
regarding waste of electrical and electronic equipment.
CATALOGUE REFERENCE
QUANTITY
USE BY
BATCH CODE
STERILIZED USING ETHYLENE OXIDE
DO NOT REUSE
MANUFACTURER
DATE OF MANUFACTURE
CAUTION : CONSULT ACCOMPANYING DOCUMENT(S)
CONSULT OPERATING INSTRUCTIONS
DO NOT USE IF PACKAGE IS DAMAGED
STORAGE CONDITIONS: • TEMPERATURE: XX°C – YY°C / XX°F – YY°F
• HUMIDITY RATE: XX% – YY%
NON-STERILE
KEEP DRY
DISCARD IN A SEPARATE COLLECTION BIN
CAUTION for USA only: US federal laws restrict this device to sale by, or on the order of, a physician.
CLASS IIA according to MDD 93/42/CEE