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注射泵和注射器檢測(cè)項(xiàng)目報(bào)價(jià)？??解決方案？??檢測(cè)周期？??樣品要求？ |
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本標(biāo)準(zhǔn)規(guī)定了分析儀器常用的基本術(shù)語(yǔ)以及電化學(xué)式分析儀器、光學(xué)式分析儀器、熱學(xué)式分析儀器、質(zhì)譜儀器、波譜儀器、色譜儀器、能譜和射線分析儀器、物性分析儀器、其他分析儀器及其輔助裝置的術(shù)語(yǔ)和定義。本標(biāo)準(zhǔn)適用于分析儀器。本標(biāo)準(zhǔn)中方括號(hào)[]內(nèi)的字是在不致混淆情況下,可省略的詞;圓括號(hào)()內(nèi)的字除說(shuō)明外,為前者的同義語(yǔ)。
本標(biāo)準(zhǔn)規(guī)定了一次性使用無(wú)菌注射器(以下簡(jiǎn)稱“注射器”)的命名、物理要求、化學(xué)要求、生物要求、包裝、標(biāo)志、貯存等。本標(biāo)準(zhǔn)適用于供抽吸液體或抽吸液體后立即注射用的手動(dòng)注射器。本標(biāo)準(zhǔn)不適用于胰島素注射器、玻璃注射器、永久帶針注射器、帶有動(dòng)力驅(qū)動(dòng)注射泵的注射器、自毀型固定劑量疫苗注射器、防止重復(fù)使用注射器、由制造廠預(yù)裝藥液的注射器以及與藥液配套的注射器等。
本標(biāo)準(zhǔn)規(guī)定了血液透析設(shè)備的術(shù)語(yǔ)和定義、分類與基本參數(shù)、要求、試驗(yàn)方法、檢驗(yàn)規(guī)則、標(biāo)志、使用說(shuō)明書(shū)和包裝、運(yùn)輸、貯存要求。 本標(biāo)準(zhǔn)適用于自動(dòng)配液的血液透析設(shè)備。 本標(biāo)準(zhǔn)不適用于: ——血液透析用水處理設(shè)備; ——腹膜透析設(shè)備; ——血液灌流、血漿置換、血漿吸附設(shè)備; ——連續(xù)性血液凈化設(shè)備。
YY/T 0573本部分規(guī)定了由高分子材料制成的公稱容量為5 mL及5 mL以上的動(dòng)力驅(qū)動(dòng)注射泵用注射器的要求，動(dòng)力驅(qū)動(dòng)注射泵用注射器應(yīng)與經(jīng)制造商確認(rèn)的注射泵配套使用。本部分不適用于胰島素注射器、玻璃注射器、由制造廠預(yù)裝藥液的注射器以及與藥液配套的注射器等。本部分不涉及注射藥液的兼容性。
本標(biāo)準(zhǔn)規(guī)定了在輸送至預(yù)設(shè)的疫苗劑量時(shí)，會(huì)自動(dòng)失效的一次性使用無(wú)菌注射器（以下簡(jiǎn)稱注射器）的術(shù)語(yǔ)和定義、命名、物理要求、化學(xué)要求、生物要求、包裝、標(biāo)志等。本標(biāo)準(zhǔn)適用于由塑料材料和不銹鋼材料制成的供抽吸疫苗或注入疫苗后立即注射用的帶針或不帶針的一次性使用無(wú)菌注射器。本標(biāo)準(zhǔn)不適用于胰島素注射器、玻璃注射器、帶動(dòng)力驅(qū)動(dòng)注射泵的注射器、不固定劑量的自毀型注射器以及預(yù)裝藥液的注射器。
本標(biāo)準(zhǔn)規(guī)定了一次性使用配藥用注射器(以下簡(jiǎn)稱“配藥器”)的要求。本標(biāo)準(zhǔn)適用于臨床抽取或配制藥液用的配藥器。本標(biāo)準(zhǔn)不適用于抽吸液體后立即注射用的手動(dòng)注射器、胰島素注射器、玻璃注射器、永久帶針注射器、帶有動(dòng)力驅(qū)動(dòng)注射泵用注射器、自毀型固定劑量疫苗注射器、防止重復(fù)使用注射器、由制造廠預(yù)裝藥液的注射器以及與藥液配套的注射器等。本標(biāo)準(zhǔn)不涉及注射藥液用過(guò)濾器。
本規(guī)范適用于醫(yī)用注射泵(以下簡(jiǎn)稱注射泵)和醫(yī)用容量式輸液泵(以下簡(jiǎn)稱輸液泵)的校準(zhǔn)。
本規(guī)范適用于離子阱、單四極桿和三重四極桿型液相色譜-質(zhì)譜聯(lián)用儀（以下簡(jiǎn)稱LC-MS)的校準(zhǔn)。
本標(biāo)準(zhǔn)規(guī)定了衛(wèi)生行業(yè)醫(yī)療器械、儀器設(shè)備（商品、物資）的分類與代碼。 本標(biāo)準(zhǔn)適用于衛(wèi)生行業(yè)各醫(yī)療、教學(xué)、科學(xué)研究和生物制品等單位對(duì)物資管理、計(jì)劃、統(tǒng)計(jì)及會(huì)計(jì)業(yè)務(wù)等使用。
SN/T 0323的本部分規(guī)定了進(jìn)出口一次性無(wú)菌注射器的抽樣、檢驗(yàn)及合格判定。本部分作為人體皮下、肌肉、靜脈等注射藥液用的一次性使用，供抽吸液體或在注入液體后立即注射用的手動(dòng)無(wú)菌注射器（以下簡(jiǎn)稱“注射器”）。本部分不適用于一次性胰島素注射器、玻璃注射器、永久帶針注射器、帶有動(dòng)力驅(qū)動(dòng)注射泵的注射器、制造廠預(yù)裝藥的注射器，以及與藥液配套的注射器。
本規(guī)程適用于醫(yī)用注射泵和輸液泵檢測(cè)儀(以下簡(jiǎn)稱檢測(cè)儀)的首次檢定、后續(xù)檢定和使用中檢查。
本標(biāo)準(zhǔn)規(guī)定了火力發(fā)電廠和核電廠水處理系統(tǒng)選用離子交換樹(shù)脂(以下簡(jiǎn)稱樹(shù)脂)的原則。本標(biāo)準(zhǔn)適用于火力發(fā)電廠和核電廠水處理系統(tǒng)用顆粒狀樹(shù)脂的選擇。
This part of ISO 7886 specifies requirements for sterile Single-use hypodermic syringes of nominal capacity 5 ml and above, made of plastics materials and intended for use with power-driven Syringe Pumps. This part of ISO 7886 does not apply to syringes for use with insulin (specified in ISO 8537), Single-use syringes made of glass (specified in ISO 595), syringes prefilled with the injection by the manufacturer and syringes supplied with the injection as a kit for filling by a pharmaeist. lt does not address compatibility with injection fluids.
This part of ISO 7886 specifies requirements for sterile single-use hypodermic syringes of nominal capacity 5 ml and above, made of plastics materials and intended for use with power-driven syringepumps.This part of ISO 7886 does not apply to syringes for use with insulin (specified in ISO 85371, single-use syringes made of glass (specified in ISO 595), syr-inges prefilled withThe injection byThe manufacturer and syringes supplied withThe injection as a kit forfilling by a pharmacist. It does not address compati-biiity with injection fluids.
This part of ISO 13628 provides general requirements and overall recommendations for development of complete subsea production systems, from the design phase to decommissioning and abandonment.This part of ISO 13628 is intended as an umbrella document to govern other parts of ISO 13628 dealing with more detailed requirements for the subsystems which typically form part of a subsea production system. However, in some areas (e.g. system design, structures, manifolds, lifting devices, and colour and marking) more detailed requirements are included herein, as these subjects are not covered in a subsystem standard.The complete subsea production system comprises several subsystems necessary to produce hydrocarbons from one or more subsea wells and transfer them to a given processing facility located offshore (fixed, floating or subsea) or onshore, or to inject water/gas through subsea wells.This part of ISO 13628 and its related subsystem standards apply as far as the interface limits described in Clause 4.Specialized equipment, such as split trees and trees and manifolds in atmospheric chambers, are not specifically discussed because of their limited use. However, the information presented is applicable to those types of equipment.If requirements as stated inThis part of ISO 13628 are in conflict with, or are inconsistent with, requirements as stated in the relevant complementary parts of ISO 13628, then the specific requirements in the complementary parts take precedence.
This part of ISO 7886 specifies requirements for sterile single-use hypodermic syringes of nominal capacity 5 ml and above. made of plastics materials and intended for use with power-driven syringe pumps. This part of ISO 7886 does not apply to syringes for use with insulin (specified in ISO 8537), single-use syringes made of glass (specified in ISO 595), syr- inges prefilled with the injection by the manufacturer and syringes supplied with the injection as a kit for filling by a pharmacist. It does not address compati- filling by a pharmacist. bility with injection fluids
