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Lowenstein Medical Allegra M30 User Manual

Lowenstein Medical Allegra M30
145 pages
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DE
EN
FR
Allegra M30
Gebrauchsanweisung
Sekretsauger
Instructions for use
Secretion aspirator
Mode dʼemploi
Aspirateur à sécrétions
Homecare
Pneumologie
Neonatologie
Anästhesie
Intensivbeatmung
Schlafdiagnostik
Service
Patientenbetreuung

Table of Contents

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Lowenstein Medical Allegra M30 Specifications

General IconGeneral
BrandLowenstein Medical
ModelAllegra M30
CategoryMedical Equipment
LanguageEnglish

Summary

1 User Information

1.1 Using this instructions for use

Guidance on how to effectively use the instruction manual for the device.

1.2 Icons

Explanation of symbols and their meanings used throughout the manual, covering device components and operation.

1.3 Symbol convention

Defines terms and abbreviations used in the manual, relating to device symbols and functions.

1.4 Glossary

Provides a list of terms and their definitions relevant to the device and its operation.

1.5 Purpose

Outlines the intended use and scope of the Allegra M30 secretion aspirator.

1.5.1 Intended use

Details the intended application and typical usage areas of the secretion aspirator Allegra M30.

1.5.2 Essential features

Highlights the key functional capabilities of the secretion aspirator, such as vacuum and flow generation.

1.5.3 Applied parts

Identifies which parts of the device are considered applied parts, specifically Type BF.

1.5.4 Indications

Lists the medical conditions and situations for which the secretion aspirator is indicated.

1.5.5 Contraindications

Specifies the applications and medical conditions for which the device is not suitable.

1.5.6 Restrictions on use

Outlines specific environments or conditions where the device's use is restricted or not recommended.

1.6 Basic safety instructions - ATTENTION!

Critical safety warnings regarding power supply, application conditions, handling of germs, and physical hazards.

Device Safety: Accessories, Connections, and Heat

Risks from improper accessories, connections, heat, and handling, plus power supply inspection.

Physiological Effects and Liquid Ingress Risks

Discusses potential patient effects, unobvious risks, and hazards related to liquid ingress.

2 Product Description

2.1 Whole view of the ME system

Provides detailed diagrams and labels for both reusable and disposable systems of the secretion aspirator.

2.2 Scope of delivery, basic device

Lists all components included in the basic package of the secretion aspirator Allegra M30.

2.3 Product properties

Details the key technical and operational characteristics of the Allegra M30, including its design and performance.

2.4 Information on the bacterial filter

Explains the function, importance, and handling of the integrated bacterial filter for safe operation.

2.5 Information on the battery

Covers battery specifications, charging procedures, and maintenance for the device's power source.

2.6 Warranty

Outlines the warranty terms and conditions for the secretion aspirator Allegra M30 and its components.

3 Operation

3.1 Set-up and startup

Step-by-step instructions for connecting and initiating the operation of the secretion aspirator Allegra M30.

3.2 Startup

Guides the user through the initial startup process, including unpacking and essential preliminary checks.

3.3.1 Control elements and indicators

Identifies and explains the function of all buttons, lights, and indicators on the device's control panel.

3.3.2 Setting the vacuum

Instructions on how to adjust the vacuum level, including fine adjustments using the fingertip air opening.

3.3.3 Aspiration

Procedures for performing the aspiration process, including important notes on filter and battery status.

3.3.4 Replacement of the disposable secretion canister

Step-by-step guide for safely replacing the disposable liner and associated components.

3.4 Decommissioning

Procedures for safely shutting down and preparing the device for storage or disposal.

4 Maintenance

4.1 Cleaning and care in outpatient and inpatient care

Guidelines for cleaning and disinfecting the device and its accessories in clinical settings.

4.2 Cleaning and care in the homecare area

Specific cleaning and care instructions tailored for homecare use of the device.

4.3 Further use of the device

Information and procedures for passing the device on for continued use by other patients.

4.4 Maintenance and service

Guidelines for routine maintenance, service, and precautions regarding device modifications and unauthorized repairs.

5 Troubleshooting

Malfunction, Display, Probable Cause, and Remedy

A table detailing common device malfunctions, their indicators, likely causes, and recommended solutions.

6 Transport, storage and disposal

6.1 Decontamination prior to shipment

Procedures for cleaning and disinfecting the device before it is shipped or returned.

6.2 Storage

Recommendations for storing the device, including battery charging and environmental conditions.

6.3 Disposal

Guidelines for the proper disposal of the device and its components according to environmental regulations.

7 Technical data

Technical Specifications Overview

A comprehensive list of technical specifications for the Allegra M30, including performance, dimensions, and environmental requirements.

8 EMC information

8.1 Electromagnetic environment for operation

Specifies the intended electromagnetic environment for operating the device safely and effectively.

8.2 Handling of electromagnetic interactions

Advice on managing potential electromagnetic interference between the device and other equipment.

8.3 List of all cables and transformers replaceable by the user

Identifies user-replaceable cables and transformers with their specifications and maximum lengths.

9 Order information accessories

Accessory Catalog

A list of available accessories for the Allegra M30, including item numbers, descriptions, and quantities.

10 Publishing information

Manufacturer Contact Details

Provides contact information for Löwenstein Medical GmbH & Co. KG, including phone, fax, email, and web address.

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