Testing of patient sample or reference material using competitor's device (Q55157): Difference between revisions

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description / pt-brdescription / pt-br
 
A investigação empregou testes empíricos relevantes de uma amostra de paciente ou material de referência usando um dispositivo de um concorrente que é comparável ao dispositivo (geralmente um IVD) envolvido no evento adverso relatado para apoiar a identificação de possíveis causas para o evento adverso. Testes relevantes normalmente são baseados em métodos de teste usados ​​para avaliar a segurança e o desempenho, conforme descrito nos padrões relevantes mais recentes.
description / endescription / en
 
The investigation employed relevant empirical testing of a patient sample or reference material using a competitor's device that is comparable to the device (usually an IVD) involved in the reported adverse event in order to support the identification of possible causes for the adverse event. Relevant testing would typically be based on test methods used for evaluating safety and performance as described in the latest relevant standards.
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/264005294 / rank
 
Normal rank
Property / CURIE
 
CID11:XE89L
Property / CURIE: CID11:XE89L / rank
 
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Property / Canary Token
 
dki-india-XE89L
Property / Canary Token: dki-india-XE89L / rank
 
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Property / Verification Status
 
Concluído
Property / Verification Status: Concluído / rank
 
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Property / Knowledge Architect
 
Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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Property / Collection date
 
13 August 2026
Timestamp+2026-08-13T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / Collection date: 13 August 2026 / rank
 
Normal rank

Latest revision as of 02:48, 14 August 2026

The investigation employed relevant empirical testing of a patient sample or reference material using a competitor's device that is comparable to the device (usually an IVD) involved in the reported adverse event in order to support the identification of possible causes for the adverse event. Relevant testing would typically be based on test methods used for evaluating safety and performance as described in the latest relevant standards.
Language Label Description Also known as
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XE89L
    English
    Testing of patient sample or reference material using competitor's device
    The investigation employed relevant empirical testing of a patient sample or reference material using a competitor's device that is comparable to the device (usually an IVD) involved in the reported adverse event in order to support the identification of possible causes for the adverse event. Relevant testing would typically be based on test methods used for evaluating safety and performance as described in the latest relevant standards.

      Statements

      CID11:XE89L
      0 references
      dki-india-XE89L
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      Concluído
      0 references
      13 August 2026
      0 references