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Criterion Cardiac Cryoablation System CE Mark Study ID: CEMA0202 ClinicalTrials.gov ID: NCT03723070This document includes CEMA0202 Protocol (PR004382 Rev 3) o Date: 04 September 2019 o Page 35 includes
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Cryoablation system fimce mark is a unique identifier used to track cryoablation systems in the medical device industry.
Manufacturers and distributors of cryoablation systems are required to file the fimce mark.
The cryoablation system fimce mark can be filled out online through the designated regulatory agency's website.
The purpose of the cryoablation system fimce mark is to ensure traceability and safety of cryoablation systems in the market.
The information that must be reported on the cryoablation system fimce mark includes the manufacturer's name, device model, and production date.
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