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Commission Decision of 7 May 2002 on common technical specifications for in vitro-diagnostic medical devices (notified under document number C(2002) 1344) (Text with EEA relevance) (2002/364/EC) is up to date with all changes known to be in force on or before 17 August 2024. There are changes that may be brought into force at a future date.
Revised legislation carried on this site may not be fully up to date. Changes and effects are recorded by our editorial team in lists which can be found in the ‘Changes to Legislation’ area. Where those effects have yet to be applied to the text of the legislation by the editorial team they are also listed alongside the affected provisions when you open the content using the Table of Contents below.
Article 1.The technical specifications set out in the Annex to this...
COMMON TECHNICAL SPECIFICATIONS (CTS) FOR IN VITRO DIAGNOSTIC MEDICAL DEVICES
3. COMMON TECHNICAL SPECIFICATIONS (CTS) FOR PRODUCTS REFERRED TO IN ANNEX...
3.1. CTS for performance evaluation of reagents and reagent products for...
3.1.1. Devices which detect virus infections shall meet the requirements for...
3.1.2. Devices intended by the manufacturer for testing body fluids other...
3.1.3. Devices intended by the manufacturer for self-test, i.e. home use,...
3.1.4. All performance evaluations shall be carried out in direct comparison...
3.1.5. If discrepant test results are identified as part of an...
3.1.6. Performance evaluations shall be performed on a population equivalent to...
3.1.7. Positive specimens used in the performance evaluation shall be selected...
3.1.8. Sensitivity with true positives and sero-conversion samples shall be evaluated...
3.1.9. Performance evaluation of screening assays shall include 25 positive (if...
3.1.10. Negative specimens used in a performance evaluation shall be defined...
3.1.11. For performance evaluations for screening assays (Table 1) blood donor...
3.1.12. Devices shall have a specificity of at least 99,5 % on...
3.1.13. Devices shall be evaluated to establish the effect of potential...
3.1.14. For devices intended by the manufacturer to be used with...
3.1.15. For devices intended for use with plasma the performance evaluation...
3.1.16. As part of the required risk analysis the whole system...
3.1.17. If a new in vitro diagnostic medical device belonging to...
3.2. Additional requirements for HIV and HCV antigen and antibody combined...
3.3. Additional requirements for nucleic acid amplification techniques (NAT)
3.3.1. For target sequence amplification assays, a functionality control for each...
3.3.2. The analytical sensitivity or detection limit for NAT assays shall...
3.3.2a. Qualitative HIV NAT assays intended to be used to detect...
3.3.2b. Qualitative HIV NAT assays, other than virus typing assays, shall...
3.3.3. Genotype detection shall be demonstrated by appropriate primer or probe...
3.3.4. Results of quantitative NAT assays shall be traceable to international...
3.3.5. NAT assays may be used to detect virus in antibody...
3.3.6. For investigation of potential carry-over, at least five runs with...
3.3.7. The whole system failure rate leading to false-negative results shall...
3.4. CTS for the manufacturer’s release testing of reagents and reagent...
3.5. CTS for performance evaluation of reagents and reagent products for...
3.5.1. All performance evaluations shall be carried out in direct comparison...
3.5.2. If discrepant test results are identified as part of an...
3.5.3. Performance evaluations shall be performed on a population equivalent to...
3.5.4. Positive specimens used in the performance evaluation shall be selected...
3.5.5. Devices shall be evaluated to establish the effect of potential...
3.5.6. For devices intended for use with plasma the performance evaluation...
3.6. CTS for the manufacturer’s release testing of reagents and reagent...
3.7. CTS for Variant Creutzfeldt-Jakob disease (vCJD) assays for blood screening...
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