ZOLL CPR-D padz
ZOLL CPR-D padz
Product Code 8900-0800-01USA
- 1 set of CPRD-pads
- First responder kit
We recommend keeping a first responder kit with your ZOLL AED so you always have the vital accessories close to hand.
Thanks to its innovative design, the “Z” shaped ZOLL CPRD pad is a single piece accessory, allowing users to reduce rescue time and position the electrodes accurately. The built-in CPR aid directs the user where to apply pressure when delivering chest compressions and measures the effectiveness of the depth and speed providing, a voice prompt will signal if you need to adjust your method.
This kit also comes equipped with additional helpful accessories including a razor and scissors which will allow you to prepare the patient for defibrillation.
- Pre-connected to save time
How to Use
The scissors can be used to cut through the patient’s clothing if required and a razor is provided should the patient’s body hair obstruct the electrodes.
Apply the CPRD- Pad to the patient’s chest following the diagram provided and follow the instructions provided by the AED.
ZOLL electrode pads have a shelf life of approximately 5 years if unused, you can sign up for the free defibshop reminder service to be notified via email when replacements are due to be ordered, helping to keep maintenance easily managed and fuss-free.
Want to learn more about the CPRD-PAD inc First Responder Kit? Our helpful team of defibshop advisors are only a phone call away. Call 800 989 7768 to speak with us directly.
Want to know why you should choose us?
- Experienced and knowledgeable staff on-hand to offer impartial advice on all things AEDs
- We have a nationwide training network to deliver training in the use of a defib and CPR
- 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
- Over 14 years worth of experience as an AED specialist
- 5 / 5 Review Score
- Over 97% of our customers would buy from us again
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.