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EN-4

MLO Dynamic

 

User Manual

EN

•  The orthosis must be checked for pro-

per function, correct fit and potential 
damage by a doctor or orthopedic tech-
nician at regular intervals. The timing 
of these intervals has to be defined 
individually for each patient. 

•  Should the product have been  

subject to disproportionate stress,  
it must be checked for potential  
damage by an orthopedic technician 
before further use. 

•  Harmful pressure caused by the ortho-

sis may cause skin injuries or disrupt 
blood flow and must be avoided.

• 

This product is intended for use
on one person. It may not be 

reused on another person.

   Safety

•  Before this device is used, the orthosis 

has to be individually adapted to the 
patient by an experienced orthopedic 
technician and the patient has to be 
trained in the orthosis’ use according to 
the doctor’s instructions.

•  Incorrect selection, adaptation, appli-

cation, and/or failure to monitor the 
correct fit of this product may cause 
health damage. 

•  Check orthosis for damage (such as 

loose connections, fasteners, belts, 
etc.) each time it is put on. 

•   Do not remove the textile label from 

textile products.

•  In case you suspect any performance 

malfunctions (e.g. an apparent reducti-
on or lack of effect), immediately call on 
your doctor or orthopedic technician. 

•  All serious incidents that occur in 

connection with this product have to 
be reported to the Wilhelm Julius Teufel 
GmbH and the competent authority 
of the member state in which you are 
established. A „serious incident“ is any 
incident that caused, may have caused, 
or may cause, directly or indirectly, one 
of the following consequences:

  a) death of a patient, user, or other  

 persons

  b) temporary or permanent health  

  deterioration of a patient, user or  
  other persons

  c) a serious public health threat.
•  Never wear the orthosis on broken skin. 

Summary of Contents for MLO Dynamic

Page 1: ...www teufel international com www wjt ortho com MLO Dynamic Gebrauchsanweisung User Manual...

Page 2: ...aschenzuges ausgef hrt und erm glichen so die Einstel lung des gew nschten Kompressionsgrades mit minimalem Kraftaufwand Indikation Indikation Pelotte Typ I LWS Insuffizienz mit rezidivierendem Lumbag...

Page 3: ...bzw Entlordosierung des Lumbalbereiches sind im Lieferumfang drei unterschiedliche Pelottentypen enthalten Typ III in der Ausf hrung eines ber br ckungsrahmens mit seitlicher F hrung Durch Abr stung...

Page 4: ...derlich Falsche Auswahl Anpassung Anwen dung und oder mangelhafte Kontrolle der Passform des Produktes k nnen zu gesundheitlichen Sch den f hren Die Orthese vor jedem Anlegen auf Be sch digungen berpr...

Page 5: ...23 510 025 00 23 510 035 00 2XL 105 120 23 510 016 00 23 510 026 00 23 510 036 00 3XL 115 130 23 510 0XX 00 90 395 084 01 DE 5 DE 5 MLO Dynamic Gebrauchsanweisung DE REF Gr en REF mit Pelotte 27 cm R...

Page 6: ...Klickverschl ssen der Orthese beidseitig nach oben schie ben um diese zu ffnen Abb 1 3 Aufnahmezapfen der Pelotte in die Klickverschl sse der Orthese einsetzen und Verriegelung zuschieben Daf r das a...

Page 7: ...r Pelotte berpr fen ggf korrigieren Einstellen der zirkul ren Kompression 1 Griff des Seilzuges dosiert nach vorne ziehen Abb 5 2 Ggf die Seill nge im aufklettbaren Griff korrigieren Dazu den Knoten w...

Page 8: ...nd links durch die Rollen einf deln Ab schlie end verl uft die Schnur mittig durch die sen und weiter zu den F hrungslaschen sodass sie wieder verknotet werden kann Komfort Hygiene Die Orthese nicht d...

Page 9: ...rtikelnummer Seriennummer Data Matrix der UDI Gebrauchs anweisung beachten Achtung CE Kennzeichnung gem EU Verordnung 2017 745 ber Medizinprodukte MDR Einzelner Patient mehrfach anwendbar Trocken aufb...

Page 10: ...com ponents work like a pulley system this allows for the compression level to be adjusted with minimal effort Indication Indication Panel Type I Lumbar insufficiency with recurring lumbago Low back p...

Page 11: ...und the torso For unloading the lumbar region and reducing lordosis three different types of pads are included in delivery Pad III is a chairback pad which also supports the patient laterally By re du...

Page 12: ...ording to the doctor s instructions Incorrect selection adaptation appli cation and or failure to monitor the correct fit of this product may cause health damage Check orthosis for damage such as loos...

Page 13: ...035 00 2XL 105 120 23 510 016 00 23 510 026 00 23 510 036 00 3XL 115 130 23 510 0XX 00 90 395 084 01 EN 5 MLO Dynamic User Manual EN REF Sizes REF with Pad Height 27 cm REF with Pad Height 29 cm REF w...

Page 14: ...fasteners Fig 1 3 Insert the pegs on the pad into the click fasteners and close the locks To do so turn the lateral part of the orthosis in order to reach the locks better Fig 2 4 Repeat on other side...

Page 15: ...Circular Compression 1 Pull the handle of the pulley cord forward with moderate force Fig 5 2 If necessary adjust the length of the pulley cord To do so open the handle on the cord by undoing the hook...

Page 16: ...wn in the illustrations alter nately thread the cord through the rollers on the right and left side Comfort Hygiene Do not wear the orthosis directly on the skin but instead over thin clothing e g a t...

Page 17: ...umber Serial Number UDI Data Matrix Follow User Manual Caution CE MarkingAccordingtoEuropean UnionCouncilRegulation2017 745 ConcerningMedicalDevices MDR Single Patient for Multiple Use Store in a Dry...

Page 18: ...Notizen Notes...

Page 19: ...Notizen Notes...

Page 20: ...Wangen Deutschland Germany Phone 49 0 7161 15684 0 Fax 49 0 7161 15684 333 www teufel international com www wjt ortho com ORTHO 90 395 084 01 Rev 2022 06 Wilhelm Julius Teufel GmbH F r dieses Drucker...

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