共找到 19 條與 醫(yī)用加速器 相關(guān)的標(biāo)準(zhǔn),共 2 頁(yè)
本文件規(guī)定了回旋加速器分類(lèi)、物理、工程等相關(guān)的術(shù)語(yǔ)及定義。 本文件適用于回旋加速器,其他類(lèi)型加速器也可參考使用。
Terminology for cyclotron
本標(biāo)準(zhǔn)規(guī)定了超導(dǎo)回旋質(zhì)子加速器機(jī)房屏蔽的一般要求、劑量率參考控制水平、屏蔽計(jì)算和輻射監(jiān)測(cè)等要求。 本標(biāo)準(zhǔn)適用于質(zhì)子能量在 70MeV~1000MeV 范圍內(nèi)的超導(dǎo)回旋質(zhì)子加速器的輻射屏蔽設(shè)計(jì),也可用于質(zhì)子能量在 70MeV~1000MeV 范圍內(nèi)的其他類(lèi)型質(zhì)子加速器的輻射屏蔽設(shè)計(jì)。
Specification for radiation shielding of superconducting proton cyclotron
Medical electron accelerators—Functional performance characteristics and test methods
本標(biāo)準(zhǔn)規(guī)定了醫(yī)用電子加速器驗(yàn)收試驗(yàn)和周期檢驗(yàn)的性能指標(biāo)、試驗(yàn)方法、試驗(yàn)條件和檢驗(yàn)周期。 本標(biāo)準(zhǔn)適用于醫(yī)用電子加速器初次安裝后,制造方、使用方和第三方共同進(jìn)行的驗(yàn)收試驗(yàn),以及設(shè)備正常工作中,使用方進(jìn)行的周期檢驗(yàn)。 本標(biāo)準(zhǔn)適用于醫(yī)療事業(yè)中以放射治療為目的、能產(chǎn)生X一輻射和電子輻射、能量為l MeV~50 MeV的醫(yī)用電子加速器。 本標(biāo)準(zhǔn)適用于配備有等中心機(jī)架的醫(yī)用電子加速器,對(duì)非等中心設(shè)備的性能和試驗(yàn)方法亦可參照?qǐng)?zhí)行。
Medical electron accelerators acceptance and periodic tests
本標(biāo)準(zhǔn)規(guī)定了醫(yī)用電子加速器的性能指標(biāo)和試驗(yàn)方法。 本標(biāo)準(zhǔn)適用于醫(yī)療事業(yè)中以治療為目的的醫(yī)用電子加速器。 本標(biāo)準(zhǔn)適用于能產(chǎn)生X-輻射和電子輻射的醫(yī)用電子加速器,其標(biāo)稱能量為1~50MeV,在距輻射源1m處的最大劑量率為0.001~1Gy/s,正常治療距離(NTD)在50~200cm之間。本標(biāo)準(zhǔn)適用于配備有等中心機(jī)架的醫(yī)用電子加速器,對(duì)非等中心設(shè)備的性能和試驗(yàn)方法可以作適當(dāng)修正。 除非隨機(jī)文件中有其他規(guī)定,本標(biāo)準(zhǔn)適用于在下列條件的環(huán)境中安裝、使用的設(shè)備: a.溫度15~35℃ b.相對(duì)濕度30%~75% c.大氣壓7×104~11×10Pa(700~1100mbar) 隨機(jī)文件必須說(shuō)明運(yùn)輸和貯存的環(huán)境條件。 電源必須符合GB9706.1中第1.4b.2)項(xiàng)的規(guī)定。 電源必須有足夠低的內(nèi)阻使有載和空載的電壓波動(dòng)不超過(guò)±5%。 注:NTD為正常治療距離英文名稱的縮寫(xiě),下文同。
Medical electron accelerators-Functional performance characteristics and test methods
Superconducting Cyclotron Rotary Therapy Room Technical Management Requirements
Technical management requirements for superconducting cyclotron water cooling system
Superconducting Cyclotron RF Resonator Technology Management Requirements
本標(biāo)準(zhǔn)規(guī)定了超導(dǎo)回旋加速器潘寧內(nèi)離子源測(cè)試平臺(tái)磁場(chǎng)測(cè)量方法的術(shù)語(yǔ)和定義、測(cè)量原理、測(cè)量條件、測(cè)量設(shè)備、測(cè)量步驟和測(cè)量報(bào)告。 本標(biāo)準(zhǔn)適用于磁場(chǎng)強(qiáng)度為 0.5T~1T,真空度為 10-4 Pa~10-2 Pa 環(huán)境下潘寧內(nèi)離子源測(cè)試平臺(tái)的磁場(chǎng)測(cè)量。
Magnetic Field Measurement Method of Superconducting Cyclotron Penning Internal Ion Source Test Platform
Dosimetry with solid thermoluminescence detectors for photon and electron radiations in radiotherapy
Medical electron accelerators - Part 6: Electronic portal imaging device(EPID) - Constancy testing
Medical electron accelerators - Part 2: Rules for construction of structural radiation protection
この個(gè)別規(guī)格は,形式試験及ぴ現(xiàn)地試験を含んでおり,それぞれ次に示す電子加速 裝()の,製造及び設(shè)置()のある段階に適用する。
Medical electrical equipment -- Part 2-1: Particular requirements for the safety of electron accelerators in the range 1 MeV to 50 MeV
The document contains rules for installation of medical electron accelerators for use of X-radiation and electron radiation in a range of 1 MeV to 50 MeV.
Medical electron accelerators - Part 2: Radiation protection rules for installation
Medical electrical equipment - Medical electron accelerators - Functional performance characteristics; Amendment 1
The document describes the constancy tests of functional performance characteristics of medical electron accelerators in the range 1 MeV to 50 MeV. Simple test methods are given which indicate reliable the relevant changes of functional performance characteristics. The recommended test frequencies are comprehended in an annex.
Medical electron accelerator - Part 5: Constancy test of functional performance characteristics
Applies to accelerators which deliver either a X or electron radiation beam with nominal energies in the range of 1 MeV to 50 MeV at maximum absorbed dose rates between 0.001 Gys-1 and 1 Gys-1 at 1 m from the radiation source and normal treatment distanc
Medical electrical equipment; medical electron accelerators; functional performance characteristics
Medical electron accelerators.Terminology
INTRODUCTION This amendment to the Particular Standard specifies the particular requirements for the electrical and mechanical safety of MEDICAL ELECTRON ACCELERATORS. It forms a further section of a comprehensive standard for such accelerators of which Section One: General and Section Two: Radiation Safety for Equipment@ have already been issued as IEC Publication 601-2-1. This amendment to the Particular Standard contains new Sub-clauses 1.2@ 3.3.1@ 3.3.2@ 3.4 and 3.5 which are additions to Section One@ and a new Section Three giving the electrical and mechanical safety requirements for equipment. The clause numbering used in this amendment to the Particular Standard is a continuation of that of IEC Publication 601-2-1. This amendment to the Particular Standard complements the General Standard@ IEC Publication 601-1: Safety of Medical Electrical Equipment Part 1: General Requirements@ in respect of electrical and mechanical safety and should be used in conjunction with that standard. In order to facilitate its use in conjunction with IECpublication 601-1@ the table below describes the link between clauses of this Particular Standard and those of IEC Publication 601-l. A requirement of this Particular Standard replacing or modifying requirements of IEC Publication takes priority over the general requirements
Medical electrical equipment. Part 2 :. Particular requirements for medical electron accelerators in the range 1 MeV to 50 MeV. Section One: General. Section Tw
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