根據98/79/ECC（IVDD）指令附錄2確定產品分類原則對有認證需求的產品進行分類。分類的依據是產品所診斷的疾病。常見產品的分類可參考下表：
與上述診斷試劑配套使用的校準品、儀器、標本采集保存用具均屬于體外診斷器械指令管理的范疇。
對界于IVDD、MDD和常規儀器之間的產品，可參考歐盟委員會MEDDEV.2.14/1 rev1 “IVD Guidances: Borderline issues”進行分類。
IVD產品歐洲協調標準：
標準號 | 內 容 |
EN375 | Information supplied by manufacturer with IVD for professional use |
EN376 | Information supplied by manufacturer with IVD for self-testing |
EN591 | Instruction for use for IVD instruments for professional use |
EN592 | Instruction for use for IVD instruments for self-testing |
EN12287 | IVD—measure of quantities—description of reference materials |
EN12286 | IVD—measure of quantities—presentation of reference measurement procedures |
EN13532 | General requirements for IVD medical devices for self-testing |
EN13612 | Performance evaluation of IVD medical devices |
EN13641 | Elimination or reduction of risk of infection related to IVD reagents |
DRAFT prEN13975 | Sampling procedures used for acceptance testing of IVD—Statistical aspects |
DRAFT prEN14136 | Use of external quality assessment schemes in the assessment of the performance of IVD procedures |
DRAFT prEN ISO18153 | IVD—measurement of quantities—metrological traceability of values for catalytic concentration of enzymes |
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