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HOME
WHY PACEAID?
  • White Paper - Beta Test
  • An Executive Brief
  • R3 Resuscitation Standard
DETAILS
  • About Us
  • FAQs
  • Gallery
  • BTI Highlights PaceAid
  • Information for Use PDFs
FAQs - More
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  • HOME
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    • White Paper - Beta Test
    • An Executive Brief
    • R3 Resuscitation Standard
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    • BTI Highlights PaceAid
    • Information for Use PDFs
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  • HOME
  • WHY PACEAID?
    • White Paper - Beta Test
    • An Executive Brief
    • R3 Resuscitation Standard
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    • FAQs
    • Gallery
    • BTI Highlights PaceAid
    • Information for Use PDFs
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VISUAL GUIDANCE FOR CRITICAL MOMENTS

Press Release

PaceAid Launches Visual CPR Guidance Tool Supporting Guideline‑Aligned Resuscitation Through Human‑Factor Design

Find out more

Visual Guidance for Critical Moments ~ When Every Second Counts

PaceAid is a visual guidance device designed to aid rescuers when performing CPR in emergencies.

  • Imagine having a visual aid to assist in CPR by providing timed visual cues for CPR cycles.    
  • PaceAid guidance is aligned with established cardiopulmonary resuscitation (CPR) guidelines, including those published by the American Heart Association.

PaceAid offers instructional support during CPR.  

  • Place PaceAid on the victim's chest, arm, shoulder, or abdomen within direct sight of performing CPR efforts.   
  • PaceAid serves as an aid during moments of uncertainty, providing visual cues during CPR.  

PaceAid is a portable, credit card-sized device that fits easily in your wallet, purse, or pocket, making it accessible and ready to use when you need it.

  •  PaceAid is an aid and does not replace CPR training. 
  • Survival depends on multiple factors beyond device use. 

Read Bulter Technologies' Feature on PaceAid

FRESH OFF THE PRESS
eNGINEERING WITH A PURPOSEENGINEERING A MEDICAL-GRADE SMART LABEL FOR REAL-TIME CPR GUIDANCE

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PaceAid brought to you by Oceana Medical LLC

P.O. Box 267, Matawan, NJ, 07747

info@paceaid.com

PaceAid is a Class 1 medical device registered and listed with the FDA. FDA registration means the manufacturer has provided the required information to the FDA, but the FDA has not reviewed or approved this product for safety or efficacy. PaceAid is manufactured in accordance with current good manufacturing practices (CGMPs). 

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