Trulife Zumo Instruction Manual

Distributeur
Zumo
Instructions and User
Guide

EN
Zumo Foot van Trulife, distributeur Loth Fabenim B.V.
Zumo Foot Instructions and User Guide 3
Contents
1. Introduction ............................................................................................................................... 4
1.1 Limitations ............................................................................................................................ 4
2. Installation and Use ................................................................................................................. 5
2.1 Endoskeletal Installations ................................................................................................... 5
2.2 Color Coating ........................................................................................................................ 6
3. Alignment ................................................................................................................................... 7
3.1 Bolt Hole Alignment ............................................................................................................. 7
3.2 Above Knee Alignment ........................................................................................................ 7
4. Maintenance Guidelines ........................................................................................................ 8
5. Limited Warranty ..................................................................................................................... 9

EN
Zumo Foot van Trulife, distributeur Loth Fabenim B.V.
Zumo Foot Instructions and User Guide4
Introduction
1
The Trulife Zumo is approved for use by all K3 activity users. Its composite keel
provides rollover assistance and stability. The Trulife Zumo is available in a 9.5mm -
3/8” heel rise with two color options.
Product Code SZM450 SZM453
Description Light Dark
Heel Rise 9.5mm - 3/8” 9.5mm - 3/8”
Patient Weight 205 kg / 450 lb 205 kg / 450 lb
Foot Sizes 25-30 cm 25-30 cm
1.1 Limitations
The Trulife Zumo cannot be used with R.O.L. rotators or other devices that require
modication of the keel.

EN
Zumo Foot van Trulife, distributeur Loth Fabenim B.V.
Zumo Foot Instructions and User Guide 5
Installation and Use
2
Recommended installation and use procedures must be followed for maximum
safety and service life.
The Trulife Zumo comes pre-assembled with a Trulife spacer, foot pyramid and foot
bolt.
WARNING: Never modify the keel. It will void the warranty and can cause
bolt or keel failure. If you must alter the form of the foot, be sure not to
grind on the keel.
WARNING: Never re-drill the mounting hole.
WARNING: Never modify the spacer. It will void the warranty and may
cause failure.
WARNING: Use only bolts supplied by Trulife. Use of unapproved bolts will
void the warranty and can cause bolt failure.
2.1 Endoskeletal Installations
When using the Trulife Zumo with a Trulife Endoskeletal Cosmesis, remove the foot
from the endoskeletal limb. Completely rough the mounting surface of the foot and
cosmesis. Remove all foam particles from the abraded surfaces. If desired, apply
small reference marks to the mounting surfaces to facilitate careful matching of the
surfaces. Apply a thin layer of contact cement to each surface and allow it to dry.
Apply a second layer of contact cement and allow to dry. Match the two surfaces
carefully and press them together tightly both on the outside and inside of the seam.

EN
Zumo Foot van Trulife, distributeur Loth Fabenim B.V.
Zumo Foot Instructions and User Guide6
Installation and Use
2
2.2 Color Coating
Before applying color coating to the foot, remove any remaining mold release from
the cosmesis with naphtha. Naphtha is recommended to improve the adhesion of
color coating, but alcohol can be used as well.

EN
Zumo Foot van Trulife, distributeur Loth Fabenim B.V.
Zumo Foot Instructions and User Guide 7
Alignment
3
The recommendations in this guide provide reliable starting points for static
alignment of the Trulife Zumo. Since each patient is unique, nal alignment may
require additional adjustment.
3.1 Bolt Hole Alignment
To establish anterior/posterior placement of the
foot, place the ankle bolt hole 12-14 mm (1/2”)
posterior to the midline of the socket. To establish
medial/lateral placement of the foot, position
the ankle bolt hole in line with the midline of the
proximal socket.
3.2 Above Knee Alignment
Use standard foot alignment procedures when
installing the Trulife Zumo.

EN
Zumo Foot van Trulife, distributeur Loth Fabenim B.V.
Zumo Foot Instructions and User Guide8
Maintenance Guidelines
4
Foot assembly should be inspected after first 30 days of use.
Inspect entire prosthesis for wear during normal consultations.
Periodically check the bolt for loosening. Retighten to 59Nm (44 ft-lbs) if loose.
WARNING: Looseness of foot bolt may lead to bolt failure.

EN
Zumo Foot van Trulife, distributeur Loth Fabenim B.V.
Zumo Foot Instructions and User Guide 9
Limited Warranty
5
Trulife warrants that the PRODUCT will be free from defects in material and
workmanship from the date of installation for the warranty period stated on the
PRODUCT warranty card.
This warranty will not apply if the PRODUCT has been damaged by misuse, abuse,
neglect, improper care, failure to follow instructions, abnormal wear and tear, or in
the event that the PRODUCT has been modied/repaired by persons unauthorized
by Trulife.
If a defect in material or workmanship is found during the warranty period, Trulife
will, at Trulife’s option, either repair or replace the product. If it is not possible to
repair or replace the product, Trulife will be limited to refunding the purchase price.
Trulife will not be liable under any legal theory for any direct, indirect, special,
incidental or consequential damages arising from the use of or inability to use this
product.
The application guidelines for this Trulife product are for the use of and by a
certied, qualied practitioner only. Patients are not to attempt to apply or adjust
the item unless expressly instructed to do so by the practitioner responsible for
the prescription and/or initial tting of the device. All patient questions should be
referred to the practitioner and not to the manufacturer. The manufacturer warrants
only that the enclosed product has been inspected for quality and can be eective
for certain indications, but nal decisions and ongoing monitoring must be made by
the prosthetic professional(s) prescribing and/or tting the device to determine its
eectiveness for an individual patient. Patient compliance is an integral part of the
entire protocol and must be adhered to in order to avoid potential problems and to
maximize the eectiveness of the prescribed product.
As a condition of the sale of any Trulife product, this prosthesis is restricted to a
“Single Patient Use Only” by the originally tted patient in order to protect the care
provider and the patient against potentially adverse consequences of infectious
disease transmission, material instability in adapting to the conguration of the
original user and/or decrease in eectivity. Any express or implied warranties are
voided if the product is reused or tted to another patient. Additionally, a license of
right to use under any relevant patents pertaining to the product is terminated with
the cessation of use by the original patient. As with all Trulife products, this product
must be prescribed and applied by a qualied practitioner to determine it meets the
needs of the particular patient and accomplishes the desired results.

Please contact us if you nd any page missing or disordered.
Contact Loth Fabenim B.V.
De Liesbosch 14-G
3439 LC Nieuwegein, THE NETHERLANDS
Tel: [phone]
Fax: [phone]
Email: [email protected]
www.lothfabenim.nl
Manufacture
Trulife
2010 East High Street
Jackson, MI 49203
USA
Tel: [phone]
Email: [email protected]
www.trulife.com
Authorized representative for EU countries
MDSS GmbH
Schigraben 41
30175 Hannover
Germany
Tel: [phone]
Email: [email protected]
www.mdss.com