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人工耳蜗植入系统检测

发布时间:2024-05-27 17:49:26 - 更新时间:2024年06月29日 15:22

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KS P 1973-2018 压电基底膜的一般要求

General requirement of piezoelectric artificial basilar membrane based cochlear implant system

YY 0989.7-2017 手术物有源式医疗器械第7部分:的专用要求

Surgical implants Active implantable medical devices Part 7: Specific requirements for cochlear implant systems

NF EN 45502-2-3:2010 有源式医疗器械 - 第 2-3 部分:和听觉脑干的特殊要求

Dispositifs médicaux implantables actifs - Partie 2-3 : exigences particulières pour les systèmes d'implant cochléaire et les systèmes d'implant auditif du tronc cérébral

NF EN ISO 14708-7:2022 外科物 - 有源式医疗器械 - 第 7 部分:和听觉脑干的特殊要求

Implants chirurgicaux - Dispositifs médicaux implantables actifs - Partie 7 : Exigences particulières pour les systèmes d'implant cochléaire et d'implant auditif du tronc cérébral

T/ZZB 2012-2020

本文件规定了人工耳蜗的术语和定义、基本要求、技术要求、试验方法、检验规则、标志、包装、运输、贮存和质量承诺。 本文件适用于年龄在12个月及以上的重度和极重度感音神经性耳聋患者适用的人工耳蜗(包括植入部分和非植入部分

Cochlear implants

EN ISO 14708-7:2022 外科物.有源可医疗装置.第7部分:的详细要求

This document specifies requirements that are applicable to those active implantable medical devices that are intended to treat hearing impairment via

Implants for surgery - Active implantable medical devices - Part 7: Particular requirements for cochlear and auditory brainstem implant systems (ISO 14708-7:2019)

ISO 14708-7:2013 外科物.有源可医疗装置.第7部分:的详细要求

This part of ISO 14708 specifies requirements that are applicable to those active implantable medical devices that are intended to treat hearing

Implants for surgery - Active implantable medical devices - Part 7: Particular requirements for cochlear implant systems

BS EN 45502-2-3:2010 有源可医疗器械.和听觉脑干的详细要求

This Part 2-3 of EN 45502 specifies requirements that are applicable to those ACTIVE IMPLANTABLE MEDICAL DEVICES that are intended to treat hearing

Active implantable medical devices - Particular requirements for cochlear and auditory brainstem implant systems

18/30357717 DC BS EN ISO 14708-7 用于手术的物 有源式医疗设备 第7部分:的特殊要求

BS EN ISO 14708-7. Implants for surgery. Active implantable medical devices. Part 7. Particular requirements for cochlear implant systems

ISO 14708-7:2019 外科物.有源医疗器械.第7部分:和听觉脑干的特殊要求

This document specifies requirements that are applicable to those active implantable medical devices that are intended to treat hearing impairment via

Implants for surgery — Active implantable medical devices — Part 7: Particular requirements for cochlear and auditory brainstem implant systems

BS EN ISO 14708-7:2022 用于手术的物 有源式医疗器械 和听觉脑干的特殊要求

1   Scope This document specifies requirements that are applicable to those active implantable medical devices that are intended to treat

Implants for surgery. Active implantable medical devices - Particular requirements for cochlear and auditory brainstem implant systems

UNE-EN ISO 14708-7:2023 手术物 有源式医疗器械 第7部分:和听觉脑干的特殊要求

Implants for surgery - Active implantable medical devices - Part 7: Particular requirements for cochlear and auditory brainstem implant systems (ISO 14708-7:2019)

NF C74-502-2-3*NF EN 45502-2-3:2010 可的有源医疗器件 第2-3部分:和脑干的详细要求

Active implantable medical devices - Part 2-3 : particular requirements for cochlear and auditory brainstem implant systems

EN 45502-2-3:2010 活动可医疗器件.第2-3部分:和听性脑干的详细要求

This Part 2-3 of EN 45502 specifies requirements that are applicable to those ACTIVE IMPLANTABLE MEDICAL DEVICES that are intended to treat hearing

Active implantable medical devices - Part 2-3: Particular requirements for cochlear and auditory brainstem implant systems

DS/EN 45502-2-3:2010 有源式医疗设备 第 2-3 部分:和听觉脑干的特殊要求

This Part 2-3 of EN 45502 specifies requirements that are applicable to those ACTIVE IMPLANTABLE MEDICAL DEVICES that are intended to treat hearing

Active implantable medical devices - Part 2-3: Particular requirements for cochlear and auditory brainstem implant systems

KS P 1973-2018 压电基底膜的一般要求

General requirement of piezoelectric artificial basilar membrane based cochlear implant system

YY 0989.7-2017 手术物有源式医疗器械第7部分:的专用要求

Surgical implants Active implantable medical devices Part 7: Specific requirements for cochlear implant systems

NF EN 45502-2-3:2010 有源式医疗器械 - 第 2-3 部分:和听觉脑干的特殊要求

Dispositifs médicaux implantables actifs - Partie 2-3 : exigences particulières pour les systèmes d'implant cochléaire et les systèmes d'implant auditif du tronc cérébral

NF EN ISO 14708-7:2022 外科物 - 有源式医疗器械 - 第 7 部分:和听觉脑干的特殊要求

Implants chirurgicaux - Dispositifs médicaux implantables actifs - Partie 7 : Exigences particulières pour les systèmes d'implant cochléaire et d'implant auditif du tronc cérébral

T/ZZB 2012-2020

本文件规定了人工耳蜗的术语和定义、基本要求、技术要求、试验方法、检验规则、标志、包装、运输、贮存和质量承诺。 本文件适用于年龄在12个月及以上的重度和极重度感音神经性耳聋患者适用的人工耳蜗(包括植入部分和非植入部分

Cochlear implants

EN ISO 14708-7:2022 外科物.有源可医疗装置.第7部分:的详细要求

This document specifies requirements that are applicable to those active implantable medical devices that are intended to treat hearing impairment via

Implants for surgery - Active implantable medical devices - Part 7: Particular requirements for cochlear and auditory brainstem implant systems (ISO 14708-7:2019)

ISO 14708-7:2013 外科物.有源可医疗装置.第7部分:的详细要求

This part of ISO 14708 specifies requirements that are applicable to those active implantable medical devices that are intended to treat hearing

Implants for surgery - Active implantable medical devices - Part 7: Particular requirements for cochlear implant systems

BS EN 45502-2-3:2010 有源可医疗器械.和听觉脑干的详细要求

This Part 2-3 of EN 45502 specifies requirements that are applicable to those ACTIVE IMPLANTABLE MEDICAL DEVICES that are intended to treat hearing

Active implantable medical devices - Particular requirements for cochlear and auditory brainstem implant systems

18/30357717 DC BS EN ISO 14708-7 用于手术的物 有源式医疗设备 第7部分:的特殊要求

BS EN ISO 14708-7. Implants for surgery. Active implantable medical devices. Part 7. Particular requirements for cochlear implant systems

ISO 14708-7:2019 外科物.有源医疗器械.第7部分:和听觉脑干的特殊要求

This document specifies requirements that are applicable to those active implantable medical devices that are intended to treat hearing impairment via

Implants for surgery — Active implantable medical devices — Part 7: Particular requirements for cochlear and auditory brainstem implant systems

BS EN ISO 14708-7:2022 用于手术的物 有源式医疗器械 和听觉脑干的特殊要求

1   Scope This document specifies requirements that are applicable to those active implantable medical devices that are intended to treat

Implants for surgery. Active implantable medical devices - Particular requirements for cochlear and auditory brainstem implant systems

UNE-EN ISO 14708-7:2023 手术物 有源式医疗器械 第7部分:和听觉脑干的特殊要求

Implants for surgery - Active implantable medical devices - Part 7: Particular requirements for cochlear and auditory brainstem implant systems (ISO 14708-7:2019)

NF C74-502-2-3*NF EN 45502-2-3:2010 可的有源医疗器件 第2-3部分:和脑干的详细要求

Active implantable medical devices - Part 2-3 : particular requirements for cochlear and auditory brainstem implant systems

EN 45502-2-3:2010 活动可医疗器件.第2-3部分:和听性脑干的详细要求

This Part 2-3 of EN 45502 specifies requirements that are applicable to those ACTIVE IMPLANTABLE MEDICAL DEVICES that are intended to treat hearing

Active implantable medical devices - Part 2-3: Particular requirements for cochlear and auditory brainstem implant systems

DS/EN 45502-2-3:2010 有源式医疗设备 第 2-3 部分:和听觉脑干的特殊要求

This Part 2-3 of EN 45502 specifies requirements that are applicable to those ACTIVE IMPLANTABLE MEDICAL DEVICES that are intended to treat hearing

Active implantable medical devices - Part 2-3: Particular requirements for cochlear and auditory brainstem implant systems

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