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 Clinical Follow-up

Labcor provides the “Implant data” and “Event Adverse report” for clinical follow –up.

Please access

All data is confidential.

The “Implant data” form must be collected by the distributor and/or sales representative as soon as possible after the surgery. All product implant must be reported to inform the model, serial number, surgeon and date of implant.

The “Event Adverse report” form is available for report any adverse event or death that can occur follow the implantation.


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