標(biāo)準(zhǔn)解讀
GB/T 44421-2024《矯形器配置服務(wù)規(guī)范》是中國(guó)關(guān)于矯形器配置服務(wù)領(lǐng)域的一項(xiàng)國(guó)家標(biāo)準(zhǔn),旨在提升矯形器服務(wù)的質(zhì)量與安全性,確?;颊吣軌颢@得適宜、專業(yè)的矯形器配置服務(wù)。該標(biāo)準(zhǔn)詳細(xì)規(guī)定了從評(píng)估、設(shè)計(jì)、制作到后期維護(hù)等一系列服務(wù)流程中的具體要求和操作規(guī)范,以保障矯形器具的個(gè)性化、有效性和舒適性。以下是對(duì)該標(biāo)準(zhǔn)主要內(nèi)容的概述:
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服務(wù)提供方資質(zhì):明確了從事矯形器配置服務(wù)的機(jī)構(gòu)或個(gè)人應(yīng)具備的相關(guān)資質(zhì)和條件,包括專業(yè)技術(shù)人員的資格認(rèn)證、場(chǎng)所設(shè)施要求及質(zhì)量管理體系等。
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患者評(píng)估:強(qiáng)調(diào)在配置矯形器前必須對(duì)患者進(jìn)行全面評(píng)估,包括但不限于醫(yī)學(xué)診斷、身體功能狀態(tài)、生活方式以及患者的具體需求,以確保矯形器設(shè)計(jì)的針對(duì)性和合理性。
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矯形器設(shè)計(jì)與制作:規(guī)定了矯形器設(shè)計(jì)應(yīng)基于評(píng)估結(jié)果,考慮材料選擇、結(jié)構(gòu)設(shè)計(jì)、功能實(shí)現(xiàn)及患者舒適度等因素。同時(shí),對(duì)矯形器的生產(chǎn)工藝、質(zhì)量控制及檢驗(yàn)標(biāo)準(zhǔn)進(jìn)行了詳細(xì)說(shuō)明,確保產(chǎn)品安全有效。
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適配與調(diào)整:要求在矯形器完成初制后,需進(jìn)行細(xì)致的適配過(guò)程,根據(jù)患者的反饋進(jìn)行必要的調(diào)整,直至達(dá)到最佳的舒適度和功能效果。
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使用指導(dǎo)與培訓(xùn):強(qiáng)調(diào)服務(wù)提供方應(yīng)對(duì)患者及其家屬進(jìn)行矯形器正確使用、維護(hù)保養(yǎng)的指導(dǎo)和培訓(xùn),確?;颊吣苡行?、安全地使用矯形器。
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跟蹤服務(wù)與反饋:要求建立完善的跟蹤服務(wù)體系,定期對(duì)患者進(jìn)行回訪,收集使用反饋,及時(shí)解決使用過(guò)程中出現(xiàn)的問(wèn)題,并對(duì)服務(wù)進(jìn)行持續(xù)改進(jìn)。
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文檔管理與隱私保護(hù):規(guī)范了服務(wù)過(guò)程中涉及的所有文檔記錄,包括評(píng)估報(bào)告、設(shè)計(jì)圖紙、適配記錄及患者信息等的管理要求,強(qiáng)調(diào)了對(duì)患者個(gè)人信息的嚴(yán)格保密。
如需獲取更多詳盡信息,請(qǐng)直接參考下方經(jīng)官方授權(quán)發(fā)布的權(quán)威標(biāo)準(zhǔn)文檔。
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- 即將實(shí)施
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- 2024-08-23 頒布
- 2024-12-01 實(shí)施
文檔簡(jiǎn)介
ICS
11.040.40
CCS
C45
中華人民共和國(guó)國(guó)家標(biāo)準(zhǔn)
GB/T44421—2024
矯形器配置服務(wù)規(guī)范
Specificationoforthosesfittingservice
2024-08-23發(fā)布2024-12-01實(shí)施
國(guó)家市場(chǎng)監(jiān)督管理總局發(fā)布
國(guó)家標(biāo)準(zhǔn)化管理委員會(huì)
GB/T44421—2024
目次
前言
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Ⅲ
1
范圍
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1
2
規(guī)范性引用文件
······················································································
1
3
術(shù)語(yǔ)和定義
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1
4
基本要求
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2
4.1
服務(wù)機(jī)構(gòu)
·························································································
2
4.2
服務(wù)人員
·························································································
2
4.3
安全要求
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2
5
服務(wù)內(nèi)容
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2
5.1
矯形器制作與適配
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2
5.2
矯形器使用訓(xùn)練
·················································································
3
5.3
售后服務(wù)
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3
6
服務(wù)流程
······························································································
3
6.1
接待
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3
6.2
檢查評(píng)估
·························································································
3
6.3
開(kāi)具矯形器處方
·················································································
4
6.4
簽署知情同意書(shū)
·················································································
4
6.5
服務(wù)實(shí)施
·························································································
4
6.6
質(zhì)量檢驗(yàn)
·························································································
4
6.7
矯形器交付
······················································································
5
7
服務(wù)評(píng)價(jià)與改進(jìn)
······················································································
5
7.1
服務(wù)評(píng)價(jià)
·························································································
5
7.2
服務(wù)改進(jìn)
·························································································
5
7.3
投訴處理
·························································································
5
附錄A(資料性)
矯形器配置基本信息
······························································
6
附錄B(資料性)
矯形器配置檢查評(píng)估及測(cè)量表
·····················································
7
附錄C(資料性)
矯形器處方
·······································································
13
Ⅰ
GB/T44421—2024
前
言
本文件按照GB/T1.1—2020《標(biāo)準(zhǔn)化工作導(dǎo)則第1部分:標(biāo)準(zhǔn)化文件的結(jié)構(gòu)和起草規(guī)則》的規(guī)
定起草。
請(qǐng)注意本文件的某些內(nèi)容可能涉及專利。本文件的發(fā)布機(jī)構(gòu)不承擔(dān)識(shí)別專利的責(zé)任。
本文件由中華人民共和國(guó)民政部提出。
本文件由全國(guó)殘疾人康復(fù)和專用設(shè)備標(biāo)準(zhǔn)化技術(shù)委員會(huì)(SAC/TC148)歸口。
本文件起草單位:中國(guó)康復(fù)輔助器具協(xié)會(huì)、金華德仁康復(fù)輔具有限公司、鄭州品康假肢矯形器技術(shù)
有限公司、江蘇天瑞醫(yī)療器械有限公司、廈門(mén)大衛(wèi)科技有限公司、北京社會(huì)管理職業(yè)學(xué)院(民政部培訓(xùn)
中心)、中國(guó)康復(fù)研究中心、合肥九久夕陽(yáng)紅新海護(hù)理院有限公司、四川省八一康復(fù)中心(四川省康復(fù)
醫(yī)院)、上海市康復(fù)器具協(xié)會(huì)、河南省民政綜合服務(wù)中心。
本文件主要起草人:逄群、張鵬程、蔣尚武、李曉剛、張振淑、馮如智、張強(qiáng)、王林、劉文倬、
文淑君、劉夕東、徐祖義、王磊。
Ⅲ
GB/T44421—2024
矯形器配置服務(wù)規(guī)范
1范圍
本文件規(guī)定了矯形器配置服務(wù)的基本要求、服務(wù)內(nèi)容、服務(wù)流程、服務(wù)評(píng)價(jià)與改進(jìn)。
本文件適用于從事矯形器配置服務(wù)的各類機(jī)構(gòu)。
2規(guī)范性引用文件
下列文件中的內(nèi)容通過(guò)文中的規(guī)范性引用而構(gòu)成本文件必不可少的條款。其中,注日期的引用文
件,僅該日期對(duì)應(yīng)的版本適用于本文件;不注日期的引用文件,其最新版本(包括所有的修改單)適用
于本文件。
GB/T14191.1假肢學(xué)和矯形器學(xué)術(shù)語(yǔ)第1部分:體外肢體假肢和體外矯形器的基本術(shù)語(yǔ)
GB/T16432康復(fù)輔助器具分類和術(shù)語(yǔ)
GB/T19012質(zhì)量管理顧客滿意組織投訴處理指南
GB/T19544脊柱矯形器的分類及通用技術(shù)條件
GB/T34410上肢矯形器的分類及通用技術(shù)條件
GB/Z41083下肢矯形器的分類及通用技術(shù)條件
GB50763無(wú)障礙設(shè)計(jì)規(guī)范
3術(shù)語(yǔ)和定義
GB/T14191.1和GB/T16432界定的以及下列術(shù)語(yǔ)和定義適用于本文件。
3.1
成品矯形器finishedorthoses
批量化、系列化生產(chǎn)的矯形裝置。
3.2
預(yù)制矯形器prefabricatedorthoses
由批量生產(chǎn)的預(yù)制件按功能障礙者需求改制的矯形裝置。
3.3
定制矯形器custom-fabricatedorthoses
根據(jù)功能障礙者需求,個(gè)性化制作的
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