ulrich medical uCentrum Instructions For Use Manual page 19

PATIENT INSTRUCTIONS AND POSTOPERATIVE MEDICAL CARE
The risks of the procedure and the use of the implant as well as possible risks due to any revisions which may be necessary should be explained
to the patient in detail. The surgeon should discuss what the expected results of using this product are with the patient in detail, in particular
with regard to possible physical limitations of the product and limitations in physical activities after implantation with the product. The post-
operative degree of activity influences the lifespan of the implant and the durability of the implant in the bone. The patient must therefore
be instructed about restrictions and risks of daily activities and any special rules of behavior. The doctor's instructions are to be complied with
implicitly. Particular attention should be given to postoperative discussion and the necessity for regular medical examination.
PRODUCT COMPLAINTS:
Any dissatisfaction with the product quality, labelling or performance should be reported to ulrich medical USA immediately by the customer
or health care provider. Furthermore, if any of the implants „malfunction," (i.e., do not meet any of their performance specifications or
otherwise do not perform as intended) and may have caused or contributed to the death or serious injury of the patient ulrich medical USA
should be notified immediately by telephone, fax, or written correspondence. When filing a complaint, the name, part number and lot number
of the part should be provided along with the name and address of the person filing the complaint.
HIGHLIGHTING AND SYMBOLS
Catalogue number
Lot code
Use-by date
Manufacturer
Date of manufacture
Consult assembly and
disassembly instructions with
special cleaning instructions
For additional information and product complaints, please contact:
ulrich medical USA
18221 Edison Avenue
Chesterfield, MO 63005
Phone: 636.519.0268
Fax: 636.519.0271
This document is valid only on the date printed. If unsure of the print date, re-print to ensure use of the latest version of the IFU. The onus resides with
the user to ensure that the most up-to-date IFU is used.
!
Caution!
Single use only
Do not use if package
is damaged
Temperature limit
Caution: Federal law restricts
this device to sale by or on the
order of a physician
CE mark with identification
number of the Notified Body
19
Qty.
Quantity
Non-sterile
NON
STERILE
Consult the instructions for use
Sterilization by irradiation
MR conditional
MR
2019-05-06