File:HC Medical Device FRN Form V1 EN.pdf
Revision as of 13:58, 10 June 2021 by Hc.mdd.postmarket-postcommercialisation.dim.sc (talk | contribs) (This form is intended to be used by manufacturers and importers to report information concerning actions taken in certain foreign jurisdictions to eliminate or mitigate a serious risk of injury to human health related to the use of a medical device, as per sections 61.2 and 61.3 of the Medical Devices Regulations.)
HC_Medical_Device_FRN_Form_V1_EN.pdf (file size: 1.41 MB, MIME type: application/pdf)
Summary
This form is intended to be used by manufacturers and importers to report information concerning actions taken in certain foreign jurisdictions to eliminate or mitigate a serious risk of injury to human health related to the use of a medical device, as per sections 61.2 and 61.3 of the Medical Devices Regulations.
File history
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| Date/Time | Dimensions | User | Comment | |
|---|---|---|---|---|
| current | 13:58, 10 June 2021 | (1.41 MB) | Hc.mdd.postmarket-postcommercialisation.dim.sc (talk | contribs) | This form is intended to be used by manufacturers and importers to report information concerning actions taken in certain foreign jurisdictions to eliminate or mitigate a serious risk of injury to human health related to the use of a medical device, as per sections 61.2 and 61.3 of the Medical Devices Regulations. |
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