2005.gada 2.augusta noteikumi Nr.581 "Medicīnisko ierīču reģistrācijas, atbilstības novērtēšanas, izplatīšanas, ekspluatācijas un tehniskās uzraudzības kārtība"

This regulation establishes the formal procedures for the registration, conformity assessment, distribution, and operation of medical devices in Latvia. It ensures that all medical equipment used within the country meets safety and quality standards through strict technical supervision. Manufacturers, distributors, and healthcare providers are affected by these rules. They must comply with specific requirements for documenting device compliance and maintaining oversight throughout the product's lifecycle to ensure patient safety.