Status on Samples (Current product from LLK)
Do you have reports of biocompatibility studies according to ISO 10993 for the non-silver products available?
Do you have reports of storage tests available for the non-silver products that verify a shelf-life of 3 or 5 years (real time storage data, not only accelerated)?
Do you have a validation report for the sealing process of the non-silver products available?
Are the non-silver products already being sold into countries falling under regulation of the European Medical Device Directive (=> CE marked products)?
In general: what kind of product information for regulatory purposes do you have at hand?
How long would you need to implement a wound pad specified by Beiersdorf – e.g. current silver wound pad without silver – in your production processes?