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Instructions for Use

Adscope

®

 Stethoscope

Thank you for choosing an ADC

®

 ADSCOPE

®

 Stethoscope. Your new stethoscope 

is designed to provide unsurpassed acoustic sensitivity, unrivaled durability, and 
unparalleled comfort. Every component has been carefully designed to maximize 
performance. 

These instructions for use are for all Adscope stethoscope models: 600, 601, 
602, 603, 604, 605, 606, 608, 612, 614, 615, 618 and 619.

 

 

 
Device Description and Intended Use

 

 
This device is intended for medical diagnostic purposes only. It can be used for 
auscultation of heart, lung, bowel and other body sounds. The device is not 
designed, sold or intended for use except as indicated.   
 
 

 
 
 
 

 

 

 
 
 
 
 
 
 
General Warnings       

A warning statement in this manual identifies 

a condition or practice which, if not corrected or discontinued immediately, 
could lead to patient injury, illness, or death.

 

  

WARNING:

Never use stethoscope without eartips firmly locked in place. 

 

WARNING:

Stethoscope contains small parts which may present a choking hazard.  

 

WARNING:

Cross-contamination of the stethoscope could cause patient infection. 

Clean and disinfect stethoscope between uses as described in Cleaning, Disinfection, 
and Storage. 

 

WARNING:

Eartips can be swallowed and cause a choking hazard. Ensure all parts are 

properly attached and stored. 

 

WARNING:

Stethoscope tubing can be a strangulation hazard. Keep away from children. 

 

 
How to Use an Adjustable Frequency Chestpiece (AFD Models - 
600, 601, 603, 604, 606, 608, 612, 614, 615, 618 and 619) 

Adscopes with AFD technology provide the enhanced acoustic response of a traditional 
bell and diaphragm. A rubber gasket around the perimeter of the diaphragm allows 
you to alter the frequency response by changing the contact pressure.

 

 

 

 

 

 

 

 

 

 
Selection of a Combination Chestpiece 
(Two-sided models - 601, 602, 603, 604, 605, 
606, 608 and 619)

 

With combination stethoscopes you can select the use of 
either the diaphragm for monitoring high-frequency sounds, 
or the open bell for monitoring low-frequency response. 

 

To select a side, hold the chestpiece valve stem in one        
hand and rotate the chestpiece 180° with the other hand 
until it “clicks” into place. The stem has an engraved dot, 
which aligns with the active side. 

 

To confirm which side is activated, tap lightly on one side, then the other, to hear 
which provides the positive response.

 

 

Converting the Chestpiece (601, 608 Only) 

The 601 and 608 chestpiece drums accommodate two 
different chestpiece attachments. To attach the bell you 
must first remove the pediatric diaphragm and then thread 
the bell clockwise until tight. 

To remove pediatric diaphragm, twist in a counterclockwise direction.

 

 

Orientation of the Headset

 

The binaurals (ear tubes) are angled at 15° to         
permit a comfortable, acoustically sealed aural fit. 
Eartips should point forward, towards the bridge 
of the nose, to fit properly.

 

 

Adjusting the Spring Tension in the Headset

 

To reduce the tension, grip the binaurals firmly using both hands with fingers at 
the center of the “Y” in the tubing, thumbs at each side where the tubing 
branches out. Flex binaurals gradually 
until the desired tension is obtained. 

To increase the tension, grip the binaurals
in the hand and squeeze the binaural tubes 
together gradually.

 

CAUTION: 

Excessive adjustment could 

weaken the spring. 

(Fig. 1)

(Fig. 2)

Correct

For low-frequency response (bell phase) 
simply hold the chestpiece in place with 
light pressure. (Fig. 1)

For high-frequency monitoring (diaphragm 
phase) apply firm fingertip pressure to the 
chestpiece. (Fig. 2)

Incorrect

To reduce tension

To increase tension

Diaphragm Activated

Bell Activated

Symbol Definitions

 

The following symbols are associated with your stethoscope. 
 
 
 
 
 

Symbol     

Definition

 

 

                 

Important Warning/Caution 

 

                     

                     

 

                     
                    Phthalate Free 

                    Read instructions before use 

                    Follow instructions for use 

                   

Meets the general safety and performance 

                     requirements of Regulation (EU) 2017/745 
                     of the European Union

LATEX

Symbol      

Definition

 

                     Authorized European Representative’s 
                    Information 

 

                   Manufacturer’s Information 

                   Date of Manufacture 

                   Lot number 

                   Medical Device 

                   Unique Device Identifier 

                   Non-Sterile

Not made with natural rubber latex

LOT

9320D-00 rev 22.qxp_Layout 1  1/7/22  12:31 PM  Page 1

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