Each device including a system medical device group medical device family or medical device group family must have a name.
Medical device labeling requirements health canada.
28 medical devices deemed licensed.
Private label manufacturers must comply with the requirements of the medical devices regulations in order for private label manufacturers to fulfil their medical device application requirements health canada will accept a letter of authorization written by the original manufacturer to grant permission to health canada to cross reference the safety and effectiveness information and quality.
As per section 86 1 no person shall sell a natural health product unless it is packaged and labelled in accordance with these regulations.
Medical devices guidance documents.
They also serve to.
Health canada guidance for the labelling of medical devices guidance document date adopted.
The device licence is issued for a the device name on the label which may describe one device b an administrative grouping of devices sold for convenience under a single name or c a grouping of devices that carry.
Canadian medical device market regulator health canada now requires all class ii medical device license mdl applicants to include labeling information in their submissions.
Applicants are responsible for ensuring that the label complies with the labelling and packaging requirements set out in part 5 of the natural health products regulations nhpr specifically sections 93 94 95 and 97 if applicable.
Health canada has provided an updated application form for class ii mdls as well as for class ii mdl amendments for which device labeling is also now required.
32 1 quality management system certificate.
32 application for a medical device licence.
As it pertains to the electronic labelling e labelling of certain medical devices not sold to the general public health canada considers e labelling to refer to the information required by section 21 1 of the regulations that would ordinarily be found in the directions for use.
24 contraceptive devices advertising.
Guidance on the content of quality management system audit reports.
Iso 13485 audit guidelines.
21 labelling requirements.
How to complete the application for a new medical device licence medical device licence amendment for a private label medical device 2020 04 01 applications for medical devices under the interim order for use in relation to covid 19 guidance document 2020 03 26.
2015 07 16 i foreword guidance documents are meant to provide assistance to industry and health care professionals on how to comply with the policies and governing statutes and regulations.
26 class ii iii and iv medical devices.
General device labeling 21 cfr part 801 use of symbols.
Guidance for labeling medical devices.
10 safety and effectiveness requirements.
25 class i medical devices.
