H10: additional information was received, the convenience sticker is part of the internal process and not related to manufacturing/service labeling issue and hence this record will not be consider as a complaint.However, since an initial mdr was submitted, the file will remain assessed as a malfunction.H10: the medical device manufacturer (d3) and manufacturing location (g1) for the straub product was selected as unknown due to system limitations.The correct medical device manufacturer and manufacturing location are straub medical us.H10: d4 (expiry date: 12/2025).H11:section a through f - the information provided by bd represents all of the known information at this time.Despite good faith efforts to obtain additional information, the complainant / reporter was unable or unwilling to provide any further patient, product, or procedural details to bd.H3 other text : device pending return.
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