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Contact: MDB Policy
Date: 2005-06-01
(check one only)
Name of Device (as it appears on the current medical device licence):
Device Class (II, III or IV):
Licence No.:
(complete only the information that is changing)
Contact Name and Title:
Company ID (if known):
Company Name:
Telephone:
Fax:
E-mail:
Street:
Suite:
P.O. Box:
City:
Province/State:
Country:
Postal/Zip Code:
Reason for change (specify the nature of the proposed change, e.g., acquisition, moving, etc.):
Proposed New Name of the Private Label Medical Device:
Reason for change (provide the reason for the change in name of device):
(include an identifier for each device or medical device group listed)
Note: Use additional pages if necessary using this same format. Catalogue pages, computer printouts, etc. will not be accepted.
I, the private label manufacturer, hereby attest that: (indicate the relevant attestations)
I, the private label manufacturer, also hereby declare that the medical device named above is a private label medical device, as defined in the Guidance for Industry - Private Label Medical Devices, in that it is identical in every respect to the medical device (name of medical device manufactured by original manufacturer), manufactured by (name of the original manufacturer) and licensed by Health Canada under Licence No. (licence number for medical device manufactured by original manufacturer), except that the medical device named above is labelled with the private label manufacturer's name, address and product name and device identifier.
Name of Private Label Manufacturer's Authorized Signing Official:
Signature:
Title:
Date: