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Systems & Procedure Packs

Definition​

A system is a combination of medical devices, and/or other products, assembled to achieve a specific intended use. A procedure pack is a combination of products, at least one of which is a medical device, assembled for a specific medical or surgical procedure.

Examples​

  • Surgical trays containing instruments, drapes, and consumables pre-assembled for a specific procedure
  • Infusion sets combined with a fluid bag and related accessories
  • Wound care packs containing dressings, antiseptics, and applicators
  • Diagnostic kits combining an IVD reagent, calibrators, and controls

Regulatory requirements​

Where all components of a system or procedure pack already hold individual Device Licences (or are Class I devices), the assembler of the system/pack:

  • Is not required to obtain a new Device Licence for the combination
  • Must not modify components in a way that affects their original performance or safety
  • Must label the system/pack in compliance with MDR labelling requirements
  • Must hold an MDEL (as a distributor or manufacturer of Class I components)

If assembling a system requires modifying a component (changing its intended use, modifying its design), a new Device Licence for the modified component or the system may be required.

Sterilisation of systems/packs​

If a system or procedure pack is assembled and then sterilised by the assembler, the assembler takes on the responsibilities of a manufacturer with respect to the sterilisation process, including:

  • Sterilisation validation
  • Packaging validation
  • Labelling for sterilised products

Legislative source: Medical Devices Regulations, SOR/98-282; Health Canada guidance on systems and procedure packs