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EUDAMED last updated this device on May 11, 2026
B-0697496998251306974969982513B-06974969982513200 Tests/kit（DR1097-3）(01)06974969982513
European Medical Device Nomenclature — the EU product classification assigned to this device.
W0102030116SQUAMOUS CELL CARCINOMA ANTIGENNo certificate specifically references this device's Basic UDI-DI.
Primary placement in Germany; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | Still on market |
CN-MF-000025964No certificates registered for this manufacturer.
No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.B-06974969982414On the market25-OH Vitamin D（25-OH-Vit-D）Detection Kit （Magnetic Solid Phase Chemiluminescent Immunoassay）B-06974969981844On the market25-OH Vitamin D（25-OH-Vit-D）Detection Kit （Magnetic Solid Phase Chemiluminescent Immunoassay）B-06974969981271On the marketAnti-Müllerian Hormone (AMH) Detection Kit（Magnetic Solid Phase Chemiluminescent Immunoassay）B-06974969982711On the marketAnti-Müllerian Hormone (AMH) Detection Kit（Magnetic Solid Phase Chemiluminescent Immunoassay）B-06974969982704On the market