ISO 13485 (Clause 7.6) - Equipment Calibration Labels Template
ISO 13485 (Clause 7.6) - Equipment Calibration Labels Template
Template Overview
Template Overview
Maintain traceability and compliance in your medical device manufacturing and quality management processes with our ISO 13485:2016 Clause 7.6 Equipment Calibration Labels Template. Proper calibration labeling is essential to ensuring measurement accuracy, equipment reliability, and regulatory compliance with ISO 13485:2016, FDA 21 CFR Part 820, MDR, and IVDR.
Key Features
Key Features
✔ Pre-Designed Calibration Label Templates – Aligned with ISO 13485:2016 Clause 7.6 requirements.
✔ Calibration Status Labels – Indicate equipment status as Calibrated, Due for Calibration, Out of Calibration, or Not in Use.
✔ Customizable Fields for Key Information – Include calibration date, due date, equipment ID, and technician name.
✔ Traceability & Compliance Section – Ensure proper documentation and audit readiness.
✔ User-Friendly Digital Format – Fully customizable and printable for use in laboratories, production areas, and quality control environments.
✔ Supports Risk Management & Quality Control – Helps prevent out-of-tolerance equipment use in critical processes.
Why choose a QMS Template?
Why choose a QMS Template?
This ready-to-use label template is ideal for quality managers, calibration technicians, and regulatory teams, ensuring proper equipment monitoring and compliance with international standards.
Download the ISO 13485:2016 Equipment Calibration Labels Template today and enhance your calibration control process!
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Additional information
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About Patient Guard
QMSRegs was founded in 2020 by the Patient Guard group to help companies get their medical devices to market and achieve Medical Device compliance. Patient Guard’s consultancy services offers a cost-effective solution for all your Quality Management System needs.
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