Equipment List; Regulatory Information - MORIA Epi-K Benutzerhandbuch

2 EQUIPMENT LIST

Designation
Box of 10 Epi-K ring -1 and 10 Epi-K
TM
Box of 10 Epi-K ring 0 and 10 Epi-K
TM
Epi-K handpiece (green color)
TM
Wrench
Storage box for the Epi-K
Tonometer
EVOLUTION 3E console / footswitch Epi-K
Aspiration tubing
Disposable brush
Epi-K single use plastic ring user manual
TM
EVOLUTION 3E console user manual (serial number below 5000)
EVOLUTION 3E console user manual (serial number 5000 and above)
Annexe "Guidance and manufacturer's declaration: electromagnetic emissions and immunity"
Guidelines (A4 format)
Guidelines (pocket format)
Epi-K protocol, drug regimen and contact lens with or without the flap
TM

3 REGULATORY INFORMATION

Customer Service Information
EUROPE
USA
Electrical Safety Standard
heads
TM
heads
TM
handpiece
TM
TM
MORIA S.A.
15, rue Georges Besse - 92160 Antony - France
Téléphone : +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 CLASS IIA according to MDD 93/42/CEE
Product registered at the Food and Drug Administration (FDA):
510(k) K043183.
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.
MORIA reference
19384
19385
19342
19345C
22519512
19042
19380/19381
19138
19149
65044
65051
65060/INTL
65073
65068
65069
65071
#65044-B-02.2017 MORIA
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