Common use of Medical Devices Clause in Contracts

Medical Devices. If any of the Products are medical devices, Buyer acknowledges that it is familiar with the U.S. Safe Medical Devices Act of 1990 as amended (the “Devices Act”) and the reporting obligations imposed on device users thereunder. In this regard, Buyer agrees to notify MEDIVATORS within ten (10) days of the occurrence of any event identified in the Devices Act imposing a reporting obligation on Buyer and/or MEDIVATORS (except for events representing an imminent hazard that require notification to the United States Food and Drug Administration (the “FDA”) within seventy-two (72) hours (or such shorter time as required by law), in which case, such notice will be delivered to the FDA and MEDIVATORS within said period). Buyer will maintain adequate tracking for the Products to enable MEDIVATORS to meet the FDA requirements applicable to the tracking of medical devices.

Medical Devices. If any of the Products are medical devices, Buyer acknowledges that it is familiar with the U.S. Safe Medical Devices Act of 1990 as amended (the “Devices Act”) and the reporting obligations imposed on device users thereunder. In this regard, Buyer agrees to notify MEDIVATORS Evoqua within ten (10) days of the occurrence of any event identified in the Devices Act imposing a reporting obligation on Buyer and/or MEDIVATORS Evoqua (except for events representing an imminent hazard that require notification to the United States Food and Drug Administration (the “FDA”) within seventy-two (72) hours (or such shorter time as required by law), in which case, such notice will be delivered to the FDA and MEDIVATORS Evoqua within said period). Buyer will maintain adequate tracking for the Products to enable MEDIVATORS Evoqua to meet the FDA requirements applicable to the tracking of medical devices.

Medical Devices. If any of the Products are medical devices, Buyer acknowledges that it is familiar with the U.S. Safe Medical Devices Act of 1990 as amended (the “Devices Act”) and the reporting obligations imposed on device users thereunder. In this regard, Buyer agrees to notify MEDIVATORS EVOQUA within ten (10) days of the occurrence of any event identified in the Devices Act imposing a reporting obligation on Buyer and/or MEDIVATORS EVOQUA (except for events representing an imminent hazard that require notification to the United States Food and Drug Administration (the “FDA”) within seventy-two (72) hours (or such shorter time as required by law), in which case, such notice will be delivered to the FDA and MEDIVATORS EVOQUA within said period). Buyer will maintain adequate tracking for the Products to enable MEDIVATORS EVOQUA to meet the FDA requirements applicable to the tracking of medical devices.

Medical Devices. If any of the Products are medical devices, Buyer acknowledges that it is familiar with the U.S. Safe Medical Devices Act of 1990 as amended (the “Devices Act”) and the reporting obligations imposed on device users thereunder. In this regard, Buyer agrees to notify MEDIVATORS Evoqua within ten (10) days of the occurrence of any event identified in the Devices Act imposing a reporting obligation on Buyer and/or MEDIVATORS Evoqua (except for events representing an imminent hazard that require notification to the United States Food and Drug Administration (the “FDA”) within seventy-seventy- two (72) hours (or such shorter time as required by law), in which case, such notice will be delivered to the FDA and MEDIVATORS Evoqua within said period). Buyer will maintain adequate tracking for the Products to enable MEDIVATORS Evoqua to meet the FDA requirements applicable to the tracking of medical devices.

Medical Devices. If any of the Products are medical devices, Buyer acknowledges that it is familiar with the U.S. Safe Medical Devices Act of 1990 as amended (the “Devices Act”) and the reporting obligations imposed on device users thereunder. In this regard, Buyer agrees to notify MEDIVATORS within ten (10) days of the occurrence of any event identified in the Devices Act imposing a reporting obligation on Buyer and/or MEDIVATORS (except for events representing an imminent hazard that require notification to the United States Food and Drug Administration (the “FDA”) within seventy-two (72) hours (or such shorter time as required by law), in which case, such notice will be delivered to the FDA and MEDIVATORS within said period). Buyer will maintain adequate tracking for the Products to enable MEDIVATORS to meet the FDA requirements applicable to the tracking of medical devices.