Common use of MEDICAL APPLICATIONS Clause in Contracts

MEDICAL APPLICATIONS. In connection with any anticipated use of Products by Buyer in medical applications, unless otherwise confirmed in a written agreement executed by duly authorized representatives of Seller, Buyer acknowledges and agrees that: (a) Seller's Products are manufactured under normal industrial conditions, which may not satisfy the requirements applicable to products manufactured for certain medical applications. It is the sole responsibility of persons contemplating medical uses of Seller's Products to comply with all applicable laws, regulations, codes and standards, including but not limited to the U.S. Federal Food, Drug and Cosmetic Act and regulations of the Food and Drug Administration. Seller's Products have not been designed, manufactured, tested or qualified for use in certain medical applications (including life support systems) and Seller has not sought or received any rulings from the FDA or any other federal, state, or local government agency as to the safety, effectiveness or appropriateness of its Products for such applications. Persons intending to evaluate or to use Seller's Products for medical purposes must rely on their own medical and legal judgment without any representation on Seller's part. (b) Buyer will indemnify, defend, and hold harmless Seller and its officers, directors, employees, agents, and contractors from and against any and all losses, claims, damages, liabilities, and expenses (including reasonable attorneys' fees) arising out of or based upon any bodily injury or property damage arising from Buyer's incorporation of Products as part of any product made by Buyer for medical applications, including without limitation cardiac pacemakers, defibrillators, electrodes, leads, programmers, and catheters, and components therefor. Seller shall give Buyer written notice of any such claim and shall cooperate in the defense of such claim at Buyer's expense.

MEDICAL APPLICATIONS. In connection with any anticipated use of Products by Buyer in medical applications, unless otherwise confirmed in a written agreement executed by duly authorized representatives of Seller, Buyer Xxxxx acknowledges and agrees that: (a) Seller's ’s Products are manufactured under normal industrial conditions, which may not satisfy the requirements applicable to products manufactured for certain medical applications. It is the sole responsibility of persons contemplating medical uses of Seller's ’s Products to comply with all applicable laws, regulations, codes and standards, including but not limited to the U.S. Federal Food, Drug and Cosmetic Act and regulations of the Food and Drug Administration. Seller's ’s Products have not been designed, manufactured, tested or qualified for use in certain medical applications (including life support systems) and Seller has not sought or received any rulings from the FDA or any other federal, state, or local government agency as to the safety, effectiveness or appropriateness of its Products for such applications. Persons intending to evaluate or to use Seller's ’s Products for medical purposes must rely on their own medical and legal judgment without any representation on Seller's ’s part. (b) Buyer Xxxxx will indemnify, defend, and hold harmless Seller and its officers, directors, employees, agents, and contractors from and against any and all losses, claims, damages, liabilities, and expenses (including reasonable attorneys' ’ fees) arising out of or based upon any bodily injury or property damage arising from Buyer's ’s incorporation of Products as part of any product made by Buyer for medical applications, including without limitation cardiac pacemakers, defibrillators, electrodes, leads, and programmers, and catheters, and components therefortherefore. Seller shall give Buyer written notice of any such claim and shall cooperate in the defense of such claim at Buyer's ’s expense.

MEDICAL APPLICATIONS. In connection with any anticipated use of Products by Buyer in medical applications, unless otherwise confirmed in a written agreement executed by duly authorized representatives of Seller, Buyer acknowledges and agrees that: (a) Seller's ’s Products are manufactured under normal industrial conditions, which may not satisfy the requirements applicable to products manufactured for certain medical applications. It is the sole responsibility of persons contemplating medical uses of Seller's ’s Products to comply with all applicable laws, regulations, codes and standards, including but not limited to the U.S. Federal Food, Drug and Cosmetic Act and regulations of the Food and Drug Administration. Seller's ’s Products have not been designed, manufactured, tested or qualified for use in certain medical applications (including life support systems) and Seller has not sought or received any rulings from the FDA or any other federalotherfederal, state, or local government agency as to the safety, effectiveness or appropriateness of its Products for such applications. Persons intending to evaluate or to use Seller's ’s Products for medical purposes must rely on their own medical and legal judgment without any representation on Seller's ’s part. (b) Buyer will indemnify, defend, and hold harmless Seller and its officers, directors, employees, agents, and contractors from and against any and all losses, claims, damages, liabilities, and expenses (including reasonable attorneys' ’ fees) arising out of or based upon any bodily injury or property damage arising from Buyer's ’s incorporation of Products as part of any product made by Buyer for medical applications, including without limitation cardiac pacemakers, defibrillators, ,electrodes, leads, and programmers, and catheters, and components therefortherefore. Seller shall give Buyer written notice of any such claim and shall cooperate in the defense of such claim at Buyer's ’s expense.

MEDICAL APPLICATIONS. In connection with any anticipated use of Products by Buyer the Customer in medical applications, unless otherwise confirmed in a written agreement executed by duly authorized representatives of Seller, Buyer the Customer acknowledges and agrees that: (a) Seller's The Company’s Products are manufactured under normal industrial conditions, which may not satisfy the requirements applicable to products manufactured for certain medical applications. It is the sole responsibility of persons contemplating medical uses of Seller's the Company’s Products to comply with all applicable laws, regulations, codes and standards, including but not limited to the U.S. Federal Food, Drug and Cosmetic Act and regulations of the Food and Drug Administration. Seller's the Company’s Products have not been designed, manufactured, tested or qualified for use in certain medical applications (including life support systems) and Seller the Company has not sought or received any rulings from the FDA or any other federal, state, or local government agency as to the safety, effectiveness or appropriateness of its Products for such applications. Persons intending to evaluate or to use Seller's the Company’s Products for medical purposes must rely on their own medical and legal judgment without any representation on Seller's the Company’s part. (b) Buyer The Customer will indemnify, defend, and hold harmless Seller the Company and its officers, directors, employees, agents, and contractors from and against any and all losses, claims, damages, liabilities, and expenses (including reasonable attorneys' ’ fees) arising out of or based upon any bodily injury or property damage arising from Buyer's the Customer’s incorporation of Products as part of any product made by Buyer the Customer for medical applications, including without limitation cardiac pacemakers, defibrillators, electrodes, leads, and programmers, and catheters, and components therefortherefore. Seller The Company shall give Buyer the Customer written notice of any such claim and shall cooperate in the defense of such claim at Buyer's the Customer’s expense.

MEDICAL APPLICATIONS. In connection with any anticipated use of Products by Buyer in medical applications, unless otherwise confirmed in a written agreement executed by duly authorized representatives of Seller, Buyer acknowledges and agrees that: (a) Seller's ’s Products are manufactured under normal industrial conditions, which may not satisfy the requirements applicable to products manufactured for certain medical applications. It is the sole responsibility of persons contemplating medical uses of Seller's ’s Products to comply with all applicable laws, regulations, codes and standards, including but not limited to the U.S. Federal Food, Drug and Cosmetic Act and regulations of the Food and Drug Administration. Seller's ’s Products have not been designed, manufactured, tested or qualified for use in certain medical applications (including life support systems) and Seller has not sought or received any rulings from the FDA or any other federal, state, or local government agency as to the safety, effectiveness or appropriateness of its Products for such applications. Persons intending to evaluate or to use Seller's ’s Products for medical purposes must rely on their own medical and legal judgment without any representation on Seller's ’s part. (b) Buyer will indemnify, defend, and hold harmless Seller and its officers, directors, employees, agents, and contractors from and against any and all losses, claims, damages, liabilities, and expenses (including reasonable attorneys' ’ fees) arising out of or based upon any bodily injury or property damage arising from Buyer's ’s incorporation of Products as part of any product made by Buyer for medical applications, including without limitation cardiac pacemakers, defibrillators, electrodes, leads, and programmers, and catheters, and components therefortherefore. Seller shall give Buyer written notice of any such claim and shall cooperate in the defense of such claim at Buyer's ’s expense.

MEDICAL APPLICATIONS. In connection with any anticipated use of Products by Buyer in medical applications, unless otherwise confirmed in a written agreement executed by duly authorized representatives of except for Seller’s Precision Interconnect Products, Buyer acknowledges and agrees that: (a) Seller's ’s Products are manufactured under normal industrial conditions, which may not satisfy the requirements applicable to products manufactured for certain medical applications. It is the sole responsibility of persons contemplating medical uses of Seller's ’s Products to comply with all applicable laws, regulations, codes and standards, including but not limited to the U.S. Federal Food, Drug and Cosmetic Act and regulations of the Food and Drug Administration. Seller's ’s Products have not been designed, manufactured, tested or qualified for use in certain medical applications (including life support systems) and Seller has not sought or received any rulings from the FDA or any other federal, state, or local government agency as to the safety, effectiveness or appropriateness of its Products for such applications. Persons intending to evaluate or to use Seller's ’s Products for medical purposes must rely on their own medical and legal judgment without any representation on Seller's ’s part. (b) Buyer will indemnify, defend, and hold harmless Seller and its officers, directors, employees, agents, and contractors from and against any and all losses, claims, damages, liabilities, and expenses (including reasonable attorneys' ’ fees) arising out of or based upon any bodily injury or property damage arising from Buyer's ’s incorporation of Products as part of any product made by Buyer for medical applications, including without limitation cardiac pacemakers, defibrillators, electrodes, leads, and programmers, and catheters, and components therefortherefore. Seller shall give Buyer written notice of any such claim and shall cooperate in the defense of such claim at Buyer's ’s expense.