Our role-based focus

 

 

 

Each functional area in a MedTech company requires specific types of data, used to perform different types of analysis, and then generates function-specific reports (like a Clinical Evaluation Report, for example).
We have conducted extensive research with MedTech companies to better understand the needs of each of those areas. Our system is designed around the needs of each of these roles, to help them get their job done faster.
This is how we help those in the role of;

Regulatory Specialist

Simplify Compliance and Speed Up FDA Approvals

Navigating complex regulatory pathways can slow down approvals and increase costs. MedTech Tracker streamlines this process with analyzed regulatory data.

MedTech Roles with airport park concept

Click to enlarge

Your Challenges

  • Needs to review large amounts of data for regulatory submissions

  • Responsible for both pre-submission and post-approval compliance

  • Finding the right product codes is difficult 

  • Manual research wastes time 

  • Regulatory updates are hard to track

How MedTech Tracker Helps

  • Summarized key regulatory data, including adverse event reports.

  • Provides access to previous filings for reference

  • Supplies full texts of 510(k) and PMA approvals

  • Business Navigation Tool that helps you find the correct product codes instantly.

  • Adverse Event Monitoring used to Track safety trends 

How to Get Started

Download free samples

510(k) premarket notification for product code NUH, NGX

510K PDF

This is a 510(k) premarket notification for the device Muscle and Nerve Stimulator TENS & EMS (TP2208), Muscle and Nerve with product code NUH, NGX

510k for Transcutaneous Electronic Nerve Stimulator with product code NUH, NYN.

510K PDF

This PDF contains the 510(k) premarket notification of intent to market the device Transcutaneous Electronic Nerve Stimulator for  product code NUH, NYN.

510k and MDR for the product code GZJ

EXCEL WITH MAUDE SUMMARY

This file contains information from FDA’s MAUDE dataset for device code GZJ. It contains these sheets: 510ks: List of 510(k)s for this product code; MDR Numbers: Identifiers for adverse events assigned to this product code and the MDR_xxxx: A separate sheet with full details of each MDR.

510K review with Product Code: NUH, NGX, NYN, GZJ, IPF

510K PDF

510(k) premarket notification of intent to market the device Nooro Body & Foot Stimulator with Product Code: NUH, NGX, NYN, GZJ, IPF

PUBMED FILES FOR THE TERM TENS

EXCEL WITH PUBMED SUMMARY

This file contains information from PubMed and the content is limited to the term ‘’TENS’’

Over 200,000+ PDFs available. Still Can’t Find What You’re Looking For?

MedTech Reference Guide

MedTech Reference Guide

Gain a better understanding of your product code, access essential medicare data and reimbursement codes. Download the MedTech Reference Guide today and request your free Regulatory and Reimbursement Report to stay ahead in the industry.

"Your data can address one of the biggest challenges in MedTech, which is identifying the right product codes, understanding the mode of action, and finding the best regulatory match. This is crucial in the early stages of product development."

Philippe D. Etter

Regulatory specialist

Swiss Medical Consultants