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010   $a0-7381-0613-5
024 7 $a10.1109/IEEESTD.1997.85519
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100   $a20231208d1997      uy             0
101 0 $aeng
135   $aur|||||||||||
181   $ctxt$2rdacontent
182   $cc$2rdamedia
183   $acr$2rdacarrier
200 10$aANSI C63.18-1997 $eAmerican National Standard Recommended Practice for an On-site, Ad-Hoc Test Method for Estimating Radiated Electromagnetic Immunity of Medical Devices to Specific Radio Frequency Transmitters /$fInstitute of Electrical and Electronics Engineers
210  1$aPiscataway, NJ, USA :$cIEEE,$d1997.
215   $a1 online resource (32 pages)
330   $aGuidance is provided for health-care organizations in evaluating the radiated RF electromagnetic immunity of their existing inventories of medical devices to their existing inventories of RF transmitters, as well as to RF transmitters that are commonly available. This recommended practice can also be used for newly purchased medical devices and RF transmitters, as well as for pre-purchase evaluation. It applies to medical devices used in health-care facilities and to portable transmitters with a rated power output of 8 W or less. It does not apply to implantable medical devices, transport environments such as ambulances and helicopters, or to RF transmitters.
517 0 $aANSI C63.18-1997
606   $aMedical instruments and apparatus
606   $aElectromagnetic compatibility
615  0$aMedical instruments and apparatus.
615  0$aElectromagnetic compatibility.
676   $a681.761
801  0$bNjHacI
801  1$bNjHacl
906   $aDOCUMENT
912   $a996279868803316
996   $aANSI C63.18-1997$93647397
997   $aUNISA