Both hospital purchasers and biomedical engineers who have to maintain refurbished and reconditioned devices say they run into problems obtaining well-written maintenance manuals and the correct parts needed to keep the products in good condition. That was the message from participants at a recent FDA workshop.
The purpose of the Oct. 27-28 workshop was to discuss potential regulations or standards that might support third-party processes for reconditioning or rebuilding older devices used in hospital or clinical...
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