. Technical Service
. Technical hotline
Do you have any technical questions?
Do you need technical service?
Telephone: +49-180-5-1 ormed de
+49-180-5-1-67 63 33
Fax:
+49-180-5-3 ormed de
+49-180-5-3-67 63 33
. Shipment
To prevent damage during transport, only
use the original shipping box. These boxes
can be obtained from DJO Global.
Before packing the CPM device, set it to
the transport position (see chapter 5).
. Spare parts
Refer to the Service Manual for the most
recent list of spare parts.
When ordering spare parts, always specify:
– item
− description
− part number
− quantity
− serial number of the CPM device
Note!
Refer repairs to authorized, specially
trained sta .
DJO Global o ers service training for
your personnel.
Surcharges may apply in certain cases to
spare parts ordered in low quantities.
Item Description
Part no.
Qty
patient chip
1.
0.0034.035
card
marker pen for
2.
patient chip
0.0031.006
card
Declaration of conformity
In compliance with the Council Directive 93/42/EEC of 14 June 1993
about medical devices, the company
ORMED GmbH
Merzhauser Strasse 112
D-79100 Freiburg - Germany
declares that the products of the product line
ARTROMOT® (see Annex)
fulfill the requirements of the Council Directive 93/42/EEC of 14 June 1993,
Annex II, as well as the essential requirements of Annex I.
With reference to Rule 9 of the Directive 93/42/EEC, the product is a
device of risk class IIa.
Notified body:
DQS Medizinprodukte GmbH
0297
August-Schanz-Str. 21
60433 Frankfurt am Main, Germany
Freiburg, 4. March 2012
–––––––––––––––––––––––––––––––––––––––––
- QA Management Representative -
-Bernhard Krohne-
This certificate is valid until expiry of the certificate referred to.
(the certificate can be downloaded from: https://de.dqs-ul.com/kunden/kundendatenbank.html)
Annex:
ARTROMOT®-S PRO
ARTROMOT®-S
ARTROMOT®-S Comfort
ARTROMOT® ACTIVE-K
ARTROMOT®-K
ARTROMOT®-K
ARTROMOT®-K PRO
ARTROMOT®-K PRO Chip
ARTROMOT®-K
ARTROMOT®-K
ARTROMOT®-SP
ARTROMOT®-SP
ARTROMOT®-E
ARTROMOT®-E compact