共找到 713 条与 医疗设备通用要求 相关的标准,共 48 页
L’Association canadienne de normalisation (CSA), sous les auspices de laquelle cette Norme nationale a été préparée, a re?u ses lettres patentes en 191 9 et son accréditation au sein du Système de Normes nationales par le Conseil canadien des normes e
Medical Electrical Equipment - Part 2-40: Particular Requirements for the Safety of Electromyographs and Evoked Response Equipment First Edition
MIL-HDBK-28001, dated 30 June 1995, has been reviewed and determined to be valid for use in acquistion.
DEPARTMENT OF DEFENSE APPLICATION OF MIL-PRF-28001 USING STANDARD GENERALIZED MARKUP LANGUAGE (SGML)
This military standard (MIL-STD) is approved and will be used by the Office of the Secretary of Defense, the Military Departments, the Chairman of the Joint Chiefs of Staff (CJCS) and the Joint Staff, the Unified and Specified Commands, Department of De
INTEROPERABILITY AND PERFORMANCE STANDARD FOR THE ALL-DIGITAL TACTICAL-TO-STRATEGIC GATEWAY
This amendment forms part of MIL-N-89404, dated 15 August 1990, and is approved for use by all Departments and Agencies of the Department of Defense.
NON-SIOP OPTION (NSO) SUPPORT
In vitro diagnostic medical devices. Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology.
In vitro medical devices. Measurements of quantities in samples of biological origin. Presentation of reference measurement procedures.
VECTOR PRODUCT FORMAT [Superseded: DOD MIL-STD-600006 ADMIN NOTICE 2, DOD MIL-STD-600006 NOTICE 1, DOD MIL-STD-600006]
VECTOR PRODUCT FORMAT [Superseded: DOD MIL-STD-600006 ADMIN NOTICE 2, DOD MIL-STD-600006 NOTICE 1, DOD MIL-STD-600006]
1.1 This practice establishes essential and recommended procedures for the conduct of quality control for a Psychophysiological Detection of Deception (PDD) examination.
Standard Practice for Quality Control of Psychophysiological Detection of Deception (Polygraph) Examinations
Specifies general requirements for safety of electromedical equipment. It is a base specification in the AS/NZS 3200 series; it becomes a complete specification for an individual item of electromedical equipment. It specifies the degrees of isolation of
Medical electrical equipment - General requirements for safety - Parent Standard
This Commercial Item Description covers a human remains pouch for mortuary use.
POUCH, HUMAN REMAINS
Safety Requirements for Electrical Equipment for Measurement, Control, and Laboratory Use Part 2-042: Particular Requirements for Autoclaves and Sterilizers Using Toxic Gas for the Treatment of Medical Materials, and for Laboratory Processes First Editio
Safety Requirements for Electrical Equipment for Measurement, Control, and Laboratory Use Part 2-042: Particular Requirements for Autoclaves and Sterilizers Using Toxic Gas for the Treatment of Medical Materials, and for Laboratory Processes First Editio
L’Association canadienne de normalisation (CSA), sous les auspices de laquelle cette Norme nationale a été préparée, a re?u ses lettres patentes en 1919 et son accréditation au sein du Système de Normes nationales par le Conseil canadien des normes en
Regles De Securite Pour Appareils Electriques De Mesurage, De Regulation Et De Laboratoire Partie 2-043: Prescriptions Particulieres Pour Les Sterilisateurs A Chaleur Utilisant De L碅ir Chaud Ou Un Gaz Inerte Chaud Pour Le Traitement Des Materiels A Usag
MIL-N-89404, dated 15 August 1990, is inactive for new design and is no longer used, except for replacement purposes.
NON-SIOP OPTION (NSO) SUPPORT
MIL-W-89500, dated 18 June 1993, is inactive for new design and is no longer used, except for replacement purposes.
WORLD MAGNETIC MODEL (WMM)
Cardiac defibrillators and cardiac defibrillator-monitors
Guidelines for the Development and Use of Medical Electrical Equipment Educational Materials First Edition; CEI/IEC 1258: 1994
Guidelines for the Development and Use of Medical Electrical Equipment Educational Materials First Edition; CEI/IEC 1258: 1994
This handbook is approved for use by all Departments and Agencies of the Department of Defense (DOD).
DOD PRODUCED CD-ROM PRODUCTS
Addition: This Particular Standard applies to the safety of EQUIPMENT FOR EXTRACORPOREALLY INDUCED LITHOTRIPSY as defined in 2.1.101. The applicability of this Particular Standard is limited to components directly involved in the LITHOTRIPSY treatment, such as, but not limited to, the generator of the PRESSURE PULSE, PATIENT support device, and their interactions with imaging and monitoring devices. Other devices, such as PATIENT treatment planning computers, X-ray and ultrasonic devices, are excluded from this Standard, because they are treated in other applicable IEC standards. While this Particular Standard has been developed for EQUIPMENT intended for use in LITHOTRIPSY, it has been developed such that, as long as no other specific standards are available to be used for other medical applications of therapeutic extracorporeal PRESSURE PULSE equipment, this Standard may be used as a guideline.
Medical electrical equipment. Particular requirements for safety. Specification for equipment for extra-corporeally induced lithotripsy
This interface standard establishes the logical structure and formats for the transfer of digital information between organizations or systems exchanging digital forms of technical information.
AUTOMATED INTERCHANGE OF TECHNICAL INFORMATION
Neonatal Ventilators First Edition; General Instruction No 1
Neonatal Ventilators First Edition; General Instruction No 1
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