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The QUICKSHIELD Complete is intended to be used only with VACUETTE® Blood Collection Tubes as a system in routine venipuncture procedures. This device is to be used by properly trained healthcare professionals only in accordance with these instructions. This device is designed with a safety shield, which can be activated to cover the needle immediately following venipuncture to aid in the protection against accidental needlestick injury. VACUETTE® VISIO PLUS Blood Collection Needles are designed for use in the daily blood collection routine when delegated by a qualified practitioner. The flashback window is situated in the transparent part of the cannula hub, which assists the user to recognize successful vein penetration. They are for single-use only and should only be used by adequately trained healthcare personnel in accordance with these instructions.

The QUICKSHIELD Complete is intended to be used only with VACUETTE® Blood Collection Tubes as a system in routine venipuncture procedures. This device is to be used by properly trained healthcare professionals only in accordance with these instructions. This device is designed with a safety shield, which can be activated to cover the needle immediately following venipuncture to aid in the protection against accidental needlestick injury. VACUETTE® VISIO PLUS Blood Collection Needles are designed for use in the daily blood collection routine when delegated by a qualified practitioner. The flashback window is situated in the transparent part of the cannula hub, which assists the user to recognize successful vein penetration. They are for single-use only and should only be used by adequately trained healthcare personnel in accordance with these instructions.

The provided text is a 510(k) summary for a medical device (VACUETTE® QUICKSHIELD Complete) and does not describe a study with acceptance criteria for device performance, ground truth establishment, or sample sizes related to AI/algorithm performance.

This document is primarily concerned with establishing substantial equivalence to previously cleared predicate devices for regulatory approval, focusing on intended use, materials, and sterilization processes. It is a submission to the FDA for a new medical device, not a report on a study comparing performance against specific metrics or historical data.

Therefore, I cannot extract the requested information as it is not present in the provided text. The questions revolve around clinical study design, AI performance, and data analysis which are not discussed in this regulatory submission.

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