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. Customer hereby warrants that:
(a) Product will not, directly or indirectly, by Customer or by any third party, be used in any of the following applications without prior written approval by Supplier for each specific product and application: U.S. FDA Class I or Class II medical devices; Health Canada Class I, Class II or Class III medical devices; European Union Class I or Class II medical devices; or similar classifications by any regional, national, or local governments; film, overwrap and/or product packaging that is considered a part or component of one of the aforementioned medical devices; and packaging in direct contact with a pharmaceutical active ingredient and/or dosage form that is intended for inhalation, injection, intravenous administration, nasal spray or ophthalmic (eye) administration.
(b) Product will not, directly or indirectly, by Customer or by any third party, be used in any of the following applications: U.S. FDA Class III medical devices; Health Canada Class IV medical devices; European Class III medical devices; or similar classifications by any regional, national, or local governments; applications involving permanent implantation into the body and life-sustaining medical applications.
MEDICAL APPLICATIONS. (a) All references to U.S. FDA, Health Canada, and European Union regulations include another country’s equivalent regulatory classification. Buyer hereby warrants that Product will not, directly or indirectly, by Buyer or by any third party, be used in any of the following applications: (i) U.S. FDA Class III Medical Devices; Health Canada Class IV Medical Devices; European Class III Medical Devices; and (ii) applications involving permanent implantation (placed in natural or surgically-created openings in a body with intent to remain there for a period of greater than thirty (30) days).
MEDICAL APPLICATIONS. In connection with any anticipated use of Products by Buyer in medical applications, except for Seller’s Precision Interconnect Products, 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 relevant PRC laws and regulations, and the laws and regulations of any country into which Buyer may sell any goods that incorporate Seller’s Products, in respect of thefood, drug and cosmetic 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 relevant 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, and programmers, and components therefore. 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. Buyer hereby warrants that: 1 Product will not, directly or indirectly, by Buyer or by any third party, be used in any of the following without prior written approval by Seller for each specific Products and application: U.S. FDA Class I or Class II medical devices; Health Canada Class I, Class II or Class III medical devices; European Union Class I or Class II medical devices; or similar classifications by any regional, national, or local governments; film, overwrap and/or product packaging that is considered a part or component of one of the aforementioned medical devices; and packaging in direct contact with a pharmaceutical active ingredient and/or dosage form that is intended for inhalation, injection, intravenous administration, nasal spray or ophthalmic (eye) administration.
MEDICAL APPLICATIONS. Buyer understands that the Products are not intended for use in any medical application involving permanent implantation in the human body, or any such implantation lasting longer than 29 days, and agrees not to use any Product for any such application, or for any other application into which, to Buyer’s knowledge, Seller has previously declined to sell Products.
MEDICAL APPLICATIONS. Note 3: 1A002.
MEDICAL APPLICATIONS. The term “Medical Applications” shall mean any and all applications involving x-ray and electron treatments which utilize stereotaxic localization for the definition of target volumes including radiosurgery and stereotaxic radiotherapy.
MEDICAL APPLICATIONS. IDT grants to Isis, a non-exclusive, royalty-bearing, worldwide license to make, have made, use, offer to sell, import, and sell IDT Licensed Commercial Products for all Medical Applications (the "Medical Applications License"). Isis may at its option extend the licenses granted hereunder to an Affiliate, in which event a sublicensing fee will not be required.
MEDICAL APPLICATIONS. Hitachi’s products are not authorised for use in MEDICAL APPLICATIONS without the written consent of the appropriate officer of Hitachi’s sales company. Such use includes, but is not limited to, use in life support systems. Buyers of Hitachi’s products are requested to notify the relevant Hitachi sales offices when planning to use the products in MEDICAL APPLICATIONS. INDEX Introduction 2 CPU Overview 5 H8 Instruction set 7 Interrupts 7 Power down modes 8 H8 Peripherals 10 Timers 10 Serial Communication Interface (SCI) 13 Analog Interface 15 Interface Peripherals 16 H8/300 and H8/300L Selector Guide 19 Xxxxxxx Xxxxx 00 DTMF Generator 17 H8/300 Packaging 18 Package Diagrams 23 Example Block Diagrams 26 Ordering Information 31 H8 Supprt Tools 32 ANSI ‘C’ Compiler 32 PCE Low Cost In-Circuit Emulator 33 CIDE 34 E6000 Emulators 34 HDI 35 System Kits 36 Evaluation Boards 37 FLASH Programming Interface 37 Third Party Tools 38 W e l c o m e T o Hitachi’s H8 microcontroller family has grown to fulfil a wide range of needs in different application areas, from low cost applications such as digital cameras and electricity meters, to high performance motor control and mobile telecoms applications. The H8 family actually comprises of a number of different series of devices, all code compatable, offering different performance levels. See figure 1. There are many advantages to choosing a Hitachi Microcontroller, these include • One common architecture covering a wide variety of applications • Maintaining your investment in code for the future • Leveraging Hitachi’s expertise in low power and low cost applications • A wide range of low cost, easy to use development tools • Wide range of low cost Flash devices Due to the pressures imposed by EMC and board space constraints, on-chip memory becomes ever more important, and the H8 family has a wide range of memory technologies and sizes, including Flash, OTP and mask ROM devices, with ROM sizes from 8 kbytes to 256 kbytes, and RAM from 256 to 16 kbytes. Hitachi has two 8-bit micro- controller families aimed at different applications areas. First the H8/300, is aimed at applications in the industrial, computer and telecoms arenas where high performance is required. The second H8/300L, is aimed at telecom and consumer applications where low power and low cost are the key design criteria. The H8/300 is a powerful 8-bit CPU core optimised for ‘C’ with a general purpose register architecture. The H8/300’s are amongst the fastest 8...
