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Arm Sling Pouch
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  • Arm Sling Pouch

Arm Sling Pouch

- Support the arm and shoulder in case of conservative or surgical management

- Soft tissue injuries like strain and sprain in the shoulder joint.

- Emergency splinting to secure the arm and shoulder.

- Post casting (weight loading)

- Hemi-sling support to the subluxate shoulder following brain stroke (hemiplegia).

- Size: XXS,XS,S,M,L,XL,XXL

  

Instructions For Use ( I F U )

- Trade Name : Healthy Arm Sling pouch 

                  هيلثى أرم إسلينج  باوتش- Arabic Name :

- Registered Trade Name Of the Manufacturer :

   HEALTHY HEALTH CARE PRODUCTS

- Registered Place of Business ( Address ) :

  99 ELSEBAK ST. – MERILAND, HELIOPOLIS,

CAIRO, Egypt  

- Where Applicable :

   Home and Hospitals

Application : Application :

* Put the semi flexed elbow into the cloth pouch including lower half of upper arm ,  elbow fore arm and hand

* Apply the strap around the back of the neck

* Put the spongy pad at back of the neck

* Fasten the strap into the metal clip to adjust the suspension level

* Put the thumb into its noose .

- How Determine the suitable size ( Sizing ) ? :

 * Use the sizing chart on the package to get the suitable size

XXL

XL

L

M

S

XS

XXS

sizes

From ulnar tuberosity to radial tuberosity while the forearm is semi flexed

Measurement

In cm

32.5

30

27.5

25

22.5

20

17.5

- Lot or Serial Number :

    MM / YY

- Sterility :

 The Device is supplied unsterile

- Single use or reusable :

The device is reusable unless it is teared or become redundant .

- The duration of use : for 3 months to 6 months

- Invasive or non invasive :

The device is non invasive

The device not introduced into human body orifices

The device not absorbed by human skin or locally dispersed

- Intended Purpose :

Healthy Arm Slings are intended to elevat the upper limb to control oedema , and enhance healing and recovery following hand , forearm , elbow , upper arm and shoulder surgery , trauma or casting.

- Indications :

* Shoulder dislocations

* Hemiplegia

* Upper limb trauma

* Upper limb casting

* Post operative ( operations in upper limb )    

- Precautions :

* Be sure of right size

* Be sure of sanitary conditions ( dry & clean )

* Reusable for not more than 6 months

* The device must not be teared or redundant

- Contra indications :  

* Teared or redundant device

- Device description :

* Pouch: a non-sterile, cotton 100 % Cloth pouch , é metal clips suspended from an overhead and shoulder support .

- Suggested Training for users

The device needs no training for users

- Performance Characteristics :

* Non invasive

* Already used non sterile but can be sterilized either by Autoclave or by Ethylene Oxide or Gamma Radiation .

* Not rupture for proper strong tighten performance .

* Easy to use i . e easy to wear and easy to get off .

* Available sizes to suit all patients , both adults and children

* Material in contact with the skin is cotton 100% ( the most safest material )

* Strong materials to ensure support

- Device specification :

* Support  Upper limb (  shoulder / upper arm / elbow/ forearm / wrist / Hand )

* Allows complete free movement when intended .

* Breathable , for cool , comfortable and extended use  

* Completely washable and hygienic

- Special Facilities :

The device requires no , special facilities, special training or particular qualification of the user

- Device maintenance and calibration :

The device needs no , regular maintenance , no consumable components , and no necessary calibration or measurements

- Instructions for cleaning :

* Put the device in tape water with some detergent for a while

* Rinse the device è tape water to remove remnant for detergent

* Dry the device away from direct sunlight , in horizontal position

* No automatic washing machine

* No electric iron

- Other devices :

Not used together with other devices

- Circumstances in which the user should consult a health care professional :

Only if the device is teared , ruptured , redundant or dirt

- Any serious incident , occurred in relation to the device should be reported to :

1- The manufacturer

2- SFDA

- Date of issue : 04/2025

    

                                

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