[Certificate.ttl] Missing information compared to RFU-STR-001

[bart-tiels]

Compared to RFU-STR-001 Issue 19 of 19/06/2024, following information is missing in Certificates.ttl:

• § A.2.1 point 2: Scope of Certification by reference to the Certification Scheme (). [R3.a,R34]
• § A.2.1 point 8: Scope of Certification by reference to Exemptions from Assessment [R17]
• § A.2.1 point 9: Scope of Certification by reference to Assessment Module(s) applied for Conformity Assessment. [R3.a,R34]
• § A.2.1 point 10: Statement about the Assessment Results (NoBo statement declaring the conformity of the Interoperability Constituent/ Subsystem or its phase/part, or quality management system with the appropriate Assessment Requirements. This is the central statement of the CLD.) [R2,R10,R16,R21,R30]
• § A.2.1 point 11: Conditions and Limits of Use (See section A.1.1 above). These are often partly contained in evidence documents supplied by the applicant and partly require documentation by the NoBo where identified during the assessment.
  The set of relevant Conditions and Limits of use must be contained in the NoBo-File section 3. On the CLD the following shall be provided:
  • the most relevant Conditions and Limits of Use in plain text and
  • a reference to the NoBo-File section 3 for the full set of relevant Conditions and Limits of Use related to the object of assessment. [R3.c, R11,R22]
• § A.2.1 point 12: (Where used) Reference to Annex of CLD [R5, R14]
  See also § A.2.2 ‘Annex of CLD’:
  • § A.2.2 point 1: Type and identification number of the related CLD (see below Section B and C) [R25]
  • § A.2.2 point 2: Scope of Certification by reference to Object of Conformity Assessment: Designation of the certified Interoperability Constituent/ Subsystem Type(s) and variant(s)/versions(s) included in the certification. Identified by industry-typical and un-ambiguous denomination. This may include a reference to a separate attached document which provides a more detailed definition (e.g. a Product Type Drawing, the NoBo-File/ Documentation, the EC Assessment Report.) [R4,R12,R28]
  • § A.2.2 point 3: Conditions and Limits of use (Follow on from the same topic on the Certificate Cover page).
  • § A.2.2 point 4: Name and address of the Notified Body and its registration number at the European Commission.
  • § A.2.2 point 5: Date of issue, signature of the authorized signatory of the Notified Body.
• § A.2.1 point 13: Reference to accompanying EC Assessment Report [R5,R14,R22,R27,R31,R32]
• § A.2.1 point 14: Reference to accompanying NoBo File [R3.c,R5,R6,R7,R13,R14,R15,R18,R19,R35]
• § A.2.1 point 16: (Where applicable) Reference to superseded CLD in case of restricted or amended EC Certificate. [R37]