What to do if my Storz Medical Equipment product has failed?
If your Storz Medical Equipment product has failed, first ensure the mains plug is firmly pushed into the connection socket. Then, verify that the wall outlet has electricity. If the issue persists, it could be due to an internal fuse defect, which requires contacting Service.
Why does my Storz Medical Equipment have no suction?
If your Storz Medical Equipment unit has no suction, examine the fluid level and empty the glass if necessary. Also, clean the plunger ball and check that it moves freely. Another possible cause is a moist and impermeable bacterial filter on the suction bottle, which requires changing the bacterial filter.
How to fix inadequate suction power in Storz Medical Equipment?
If your Storz Medical Equipment exhibits inadequate suction power, check the tubing line for any leakage and replace if necessary. Also, ensure the sealing cap is correctly seated.
What to do if Storz Medical Equipment has no irrigation pressure?
If your Storz Medical Equipment has no irrigation pressure, check the tubing and connections, replacing them if necessary. If the problem persists, it may be due to defective control electronics.
General| Brand | Storz |
|---|---|
| Model | ENDOMAT SELECT UP210 |
| Category | Medical Equipment |
| Language | English |
Instructions for safe and correct operation of the product.
Explains the meaning of different danger levels in warnings.
Glossary of technical terms and abbreviations used in the manual.
Describes the primary functions and applications of the product.
Lists the medical disciplines and procedures for which the product is indicated.
Outlines situations or conditions where the product should not be used.
Specifies the qualified personnel authorized to operate the device.
Details the patient demographics for whom the product is intended.
Specifies the body areas and disciplines where the product can be applied.
Defines the environment and conditions suitable for product operation.
Defines what constitutes a serious incident as per MDR.
Provides guidelines for safe operation and handling to prevent injury.
Advises against using damaged products due to potential injury risks.
Details risks of electric shock and safety precautions for power supply.
Explains risks from liquid ingress and resulting product damage or injury.
Discusses precautions related to EMC and potential interference.
Advises on preparing for potential product malfunctions during use.
Highlights the importance of operating within specified environmental conditions.
Warns about potential interference when integrating the product into IT networks.
Prohibits product modifications to maintain safety and prevent injury.
Explains the primary functions and operational principles of the ENDOMAT SELECT.
Identifies and illustrates the main components of the ENDOMAT SELECT.
Describes the user interface of the touch screen for device control.
Explains the meaning of various symbols displayed on the touch screen.
Lists compatible devices and accessories for system integration.
Details the different ways the product can be used (irrigation/suction).
Provides detailed technical specifications and parameters of the device.
Introduces symbols used on the product packaging and device.
Explains symbols found on the product packaging.
Explains symbols directly marked on the product itself.
Specifies the required storage and operating environmental conditions.
Details the requirements for medical electrical systems and configurations.
Warns against connecting non-medical products to the system.
Provides guidance on the safe use of multiple socket outlets with the system.
Outlines the limits for electrical load when using the system.
Refers to instructions for reprocessing system components.
Covers maintenance requirements for the product and system components.
Steps for safely removing the product and accessories from packaging.
Guidelines for properly installing the product in its operating environment.
Instructions for connecting the product to power and other components.
Procedures for verifying the product's functionality before use.
Steps for powering on and initiating the product's self-test.
Guide to selecting the appropriate medical discipline and procedure.
Detailed instructions for correctly installing the disposable tubing set.
Instructions for setting up combined operation with the CALCUSON device.
Steps for installing the optional bottle holder accessory.
Steps for powering on and initiating the CALCUSON in combined use.
Guide for setting up combined operation with UNIDRIVE S III.
Steps for initiating UNIDRIVE S III for combined operation.
Instructions for setting up combined operation with UNIDRIVE S III ARTHRO.
Steps for initiating UNIDRIVE S III ARTHRO for combined operation.
Detailed steps for connecting the tubing set for indirect suction.
Detailed steps for connecting the tubing set for direct suction.
Overview of the main menu structure and access to settings.
Access to various configurable settings for the product.
Instructions for changing the device's display language.
Configuration options for brightness, volume, boost time, and units.
Procedure for adjusting height difference for accurate pressure measurement.
Information on accessing and viewing recorded system events and alarms.
How to retrieve product details like serial number and software version.
Information regarding access to service menus and password protection.
Steps to remove air from the tubing system before use.
Specific procedure for venting tubing in SURG discipline.
Procedure for venting tubing in HYS, URO, ART, and SPINE disciplines.
Procedure for venting the tubing system during suction operations.
Guide on using the device for irrigation functions.
How to set irrigation flow rates for SURG and VET SURG.
Instructions for setting irrigation flow for ENT/NEURO procedures.
How to set irrigation pressure for various medical disciplines.
Procedures for initiating and terminating irrigation operations.
Guide on using the device for suction functions.
How to set suction flow rates for various procedures and devices.
Outlines the recommended maintenance activities and intervals.
Details the specific maintenance tasks required for the product.
Describes the system's alarm and information signals.
Explains different types of audible and visual alarms.
Describes the visual indicators of alarms on the device display.
Details the characteristics of audible alarm sounds.
Procedure to verify the correct operation of the alarm system.
Explains the meaning and purpose of informational messages.
Describes visual information messages displayed on the device.
Details the characteristics of audible information signals.
Explains the availability signal indicating system readiness.
Information on the audible feedback for button presses.
Procedure to test the excess pressure alarm functionality.
Procedure to verify the correct display of information signals.
Guidelines for mandatory safety inspections according to IEC standards.
Steps for performing a visual check of the product and accessories.
Procedures for electrical safety measurements during inspection.
Steps for conducting functional tests as part of safety inspection.
Information on authorized repair procedures and contacts.
Guidance on the proper disposal of the product according to WEEE directive.
Lists available accessories, consumables, and their order numbers.
General information about the product's suitability for healthcare environments.
Details on accessories and lines necessary for EMC compliance.
Specifies compliance levels for various immunity tests.
Test levels for HF fields from wireless communication devices.
Test levels for radiated and conducted immunity.
Defines the emission class and group of the product.
Recommendations for maintaining safe distances from HF devices.
Provides common faults, their possible causes, and corrective actions.
Lists software error messages, their causes, and recommended actions.
Summarizes key warnings related to electrical shock, RF interference, and modifications.
Lists KARL STORZ subsidiaries and contact information worldwide.
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