Overseas Kit - Professional
Overseas Kit - Professional
Product Code 245
- 2 Terumo Syringe 1ml
- 2 Terumo Syringe 2ml
- 2 Terumo Syringe 5ml
- 3 Terumo Needle Blue 23g x 1"
- 3 Terumo Needle Hypodermic 21g x 1.5 3
- Terumo Needle Hypodermic Orange 25g x 5/8"
- 1 IV Cannula 18g x 45mm Green
- 2 Skin Closure Strips 6mm x 75mm (3)
- 2 Relipad Non Adherent Dressing Pads 5cm x 5cm
- 2 Relipad Non Adherent Dressing Pads 10cm x 10cm
- 1 Relitape Microporous Tape 2.5cm x 10m
- 1 Vinyl Powder-Free Medium Single (pair)
- 1 Assorted Washproof Plasters Wallet of 20
- 2 Unilet General Purpose Superlite Blood Lancets 23g
- 1 Sutures W320 Singles
- 1 Giving Set Luer Lock Vent 185cm
- 4 Reliject Swabs
This kit is designed to be used by a medical professional abroad where the sterility of medical disposables cannot be guaranteed.
The contents come handily in a versatile, compact medical bag, with 4 clear pockets and a mesh zip-up compartment, holding just about everything you could need to assist your treatment.
First Aid Essentials
Fully stocked with everything you need to assist you in an emergency situation, this compact kit comes with all the tools necessary for a medical professional, helping make the application of treatment easier and more effective.
The perfect option for doctors of administrators of professional care, this is the perfect solution when you may be out of office or are planning on going overseas to ensure you can always take action in an emergency situation.
Want to learn more about this product and its contents? The help advisors of defibshop are here to help.
With a plethora of knowledge under our belts, you can be confident no matter what your query, we’ll have the answer to assist you in finding the right products for you. To get in touch, simply call 0845 071 0830.
Want to know why you should choose us? Press play and find out more...
And if it couldn't get any better..
- We have over 50 different defibrillators available and we can help you decide the best one for you
- We have over 200 trainers nationwide to deliver nationally accredited training in the use of a defib and CPR
- Over 20 staff on hand to offer impartial advice on all things defibrillators
- Not only providing free battery and pad reminders, we also will replace your electrode pads for free if you use your defib in the first two years after purchase
Did we also mention we are an Award Winning company?
We’re sure that you have been past our Home Page, but in case you haven’t, skipping the intro and getting stuck into the world of defibrillators, we are an award winning company.
This year we added an impressive trophy to the cabinet by being listed 22nd in the ‘Great Place to Work: Best Workplaces 2014’ Small Business Category.
We also have to our name Salford Business Excellence Award Runner Up 2014 & 2012, Investors in People – Bronze Award and an Insight 100 Customer Service Award in Training Services 2013 award.
We also have a number of accreditations under our belt, including being a TQUK Diamond Approved Centre, ISO 9001 and 14001 and CIEH.
What is an IP rating?
An IP (Ingress Protection) rating classifies the degrees of protection of an electrical item against water and dust. Beginning with IP and followed by two numbers, the first digit is indicative of the item’s resistance to dust and the second is of its resistance to water. Protection against dust is measured from */ 0 up to 6, whereas protection against water is measured from */ 0 up to 8. The protection against these elements increases as the number does, with * / 0 telling us that the item has NO protection against either dust or water.
Why is this important?
The IP rating of a defib will tell you (and us!) whether it is suitable for the environment where it’s most likely to be used; for example, if there is a good chance your defib may be used in an outdoor environment, you will need a unit with a higher IP rating to ensure it can be used regardless the weather or terrain. If you are looking for a defibrillator more suitable for an indoors environment, you can afford to choose one with a lower IP rating, based on the other features that may be more suitable.
When a particular product is “approved” by the FDA, this marks the pass in the premarket approval (or PMA) application of a particular product which has been submitted to the FDA.
To receive approval of a device through a PMA application, the applicant in question must provide reasonable assurance of the device’s safety and effectiveness which is then challenged by the FDA before being approved.
Whilst all AEDs can be used to increase chances of survival and even save a life in the event of a cardiac arrest, FDA approved devices provide that extra piece of mind that the specific unit being used has undergone vigorous and substantial testing to ensure that that particular piece of equipment operates just as it should and provides the most effective care possible.
Many manufacturers perform their own tests on products, but not all defibrillators will undergo the same premarket approval as FDA approved devices and there is no guarantee or stamp of certification if testing has taken place with non-FDA approved products.