VERIFY CODE QUALITY ON MEDICAL PRODUCTS

Ensure accuracy and a high first-pass reading rate

Manufacturers and sellers of medical devices in the EU and the USA cannot afford to make mistakes in UDI marking. Integrated code verification systems are used in production to ensure that they meet all international labeling requirements and that the codes are correct and clearly readable.

© Andreas Volz
Andreas Volz

Verifiers and test systems for high first-pass reading rates

RELIABLE INSPECTION FOR UDI CODES

Ensuring high first-pass reading rates in automated UDI processes requires compliance with high code quality and applicable standards. Code verification devices from REA VERIFIER are used to ensure that markings and codes are error-free and comply with the MDR standard. Each marking receives an acceptance test report in this way.

Regardless of whether it is applied directly to the medical device or as a label: In medical technology, the UDI marking prescribed by the Medical Device Regulation 2017/745 (MDR) is used for many automated processes along the entire supply chain, for example in logistics and in the event of necessary recalls. Manufacturers therefore have to ensure high first-pass reading rates for the UDI code. A high code quality and the standard-compliant structure of the UDI code are essential for this. Special inspection systems and verifiers are used to ensure that the 1D or 2D Barcodes are error-free and comply with the MDR standards. Each medical device marking receives an acceptance test report.

What is important for testing systems?

  • Inspection of legally compliant marking
  • Traceability and quality assurance
  • Fast, reliable reading of codes
  • Reliable automatic error detection
  • Flexible, powerful and expandable software
  • Easy integration into production lines / quality assurance
  • Flexible use for different products
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Plain text check and code check

PRECISE QUALITY CONTROL FOR CODES ON MEDICAL DEVICES

With our versatile testing solutions, we support medical technology companies in complying with international marking regulations and contribute to clear product identification and patient protection.

Typical application examples for our inspection solutions

  • Reading 1D Codes and 2D Codes on medical devices and packaging
  • Plain text inspection on medical devices
  • In-line inspection including database connection and evaluation
verify 2D Code on inhaler

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GOOD TO KNOW
MDR
Medical Device Regulation

Anyone wishing to place medical devices on the market in the EU has to comply with the Medical Device Regulation MDR 2017/745. Among other things, it regulates the unique product marking by code and plain text on medical devices and their secondary packaging using Unique Device Identification (UDI).


Medical technology
Safely marking, labeling and verifying medical devices and packaging
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