DATOSPIR
· User’s Manual
EN 21
511-D00-MUM · Rev 1.01
Actions to be performed by qualified staff:
The Medical Device Directive 93/42/CEE recommends that medical devices should be
regularly checked and calibrated to assure the reliability of its funtions and the safety for
the patients and users.
This technical verification must be done every year following the Adjustment and
Verification Procedure of
DATOSPIR
, defined by the manufacturer SIBEL S.A.U.
This procedure must be performed by manufacturer’s Technical Service staff or the dealer.
This one must have written autoritation of
SIBEL S.A.U
. to perform the maintenance.
The manufacturer IS NOT liable for malfunction or damage in the device due to of faulty
maintenance performed by non certified staff.
Contact SIBEL S.A.U. After Sales Service to recieve more information about different
types of PREVENTIVE MAINTENANCE available.
4.5 CORRECTIVE MAINTENANCE
Corrective maintenance consists in repairing the device when it is no longer in service;
leaving it in good conditions for use.
If there is any failure in the device contact the
SIBEL S.A.U
After Sales Service, specifying
the anomaly occurred.