We are looking at updating the description of item 123741 as follows:
EXCEED ABT APICAL PLUG – SPARE (current)
Apical Hole Plug – 3/8 – 24 Thread (new)
The description on the label, on the Declaration of Conformity, on material brochure (surgical technique) will be updated to reflect this change where Biomet UK ltd is the legal manufacturer.
Could you let me know if this change will impact the current approval or pending approval in your country when this device is registered under Biomet UK Ltd? If yes,
- what documents will be required?
- if stock management/inventory has to be put in place?
- how long it will take to get the change approved?