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Otto Bock 17B98 Series User Manual

Otto Bock 17B98 Series
120 pages
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17B98*
Gebrauchsanweisung ................................................................ 4
Instructions for use .................................................................... 10
Instructions d'utilisation ............................................................. 15
Istruzioni per l’uso ..................................................................... 22
Instrucciones de uso ................................................................. 28
Manual de utilização .................................................................. 35
Gebruiksaanwijzing ................................................................... 41
Bruksanvisning ......................................................................... 47
Brugsanvisning ......................................................................... 53
Bruksanvisning ......................................................................... 59
Käyttöohje ................................................................................ 64
Instrukcja użytkowania ............................................................... 70
Használati utasítás .................................................................... 77
Návod k použití ......................................................................... 82
Návod na používanie .................................................................. 88
Kullanma talimatı ....................................................................... 94
Οδηγίες χρήσης ....................................................................... 100
Руководство по применению .................................................... 106
取扱説明書
............................................................................... 114
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Otto Bock 17B98 Series Specifications

General IconGeneral
BrandOtto Bock
Model17B98 Series
CategoryMedical Equipment
LanguageEnglish

Summary

Foreword

Product Description and Components

Available Sizes

Lists the different system widths and corresponding reference numbers for the orthotic ankle joints.

Components in Scope of Delivery

Details the components included in the delivery for Figure 1, including quantity and article numbers.

Components Not Included in Delivery

Lists accessories and materials that are not part of the standard product package.

Design and Fabrication

Intended Use and Indications

Indications for Use

Specifies that the orthotic ankle joints are for exclusive use in pairs for lower limb orthotic treatment.

Indications

Lists medical conditions, such as paralysis of leg muscles, for which the product is indicated.

Combination Possibilities

Mentions the compatibility of these ankle joints with other specific orthotic knee joints.

Safety Information and Warnings

Explanation of Warning Symbols

Defines the meaning of 'CAUTION' and 'NOTICE' symbols used throughout the document.

General Safety Instructions and Precautions

Covers alignment, assembly, strain, mechanical damage, environmental conditions, and thermal overloading.

Preparation and Cleaning Procedures

Parallel Alignment of Orthotic Joints

Describes the use of an alignment fixture for positioning orthotic joints on a plaster positive.

Preparing the Orthotic Ankle Joint

Details steps for securing lamination bars and mounting the ankle joint with alignment inserts.

Shaping and Securing Lamination Bars

Explains how to secure, mark, and shape lamination bars for optimal fit and bonding.

Bending Foot Stirrups

Outlines the procedure for disassembling and carefully bending the foot stirrups.

Cleaning Instructions

Provides guidance on promptly cleaning the orthosis joint with fresh water after use.

Maintenance, Disposal, and Legal Information

Maintenance Recommendations

Suggests shortening maintenance intervals based on patient load and recommends semi-annual inspections.

Disposal Guidelines

Instructs users to dispose of the product in accordance with applicable national regulations.

Liability Conditions

Defines the manufacturer's liability limits concerning product usage and modifications.

CE Conformity Declaration

Confirms compliance with European directives for medical devices and its classification.

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