VERTOS MEDICAL, INC. - BEUDAMED

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1 results · 62ms · Sources: EU EUDAMED, US FDA

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FDA FEI Number

1000036860 1 1000112877 1 1000112968 1 1000116142 1 1000120548 1 1000120613 1 1000123143 1 1000123848 1 1000124817 1 1000132435 1 1000136409 1 1000138054 1 1000160458 1 1000161215 1 1000219637 1 1000221492 1 1000244733 1 1000306139 1 1000306340 1 1000306431 1 + More FDA FEI Numbers

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1000517406 1 1017294 1 1018233 1 1018470 1 1030489 1 1032347 1 1043214 1 1045254 1 1047429 1 1048735 1 1054241 1 1055236 1 1056128 1 1058584 1 1061124 1 1061927 1 1064017 1 1123169 1 1219602 1 1219930 1 + More FDA Registration Numbers

Vertos mild Device Kit (MDK-0002)

FDA Class 2 ·Orthopedic

Data last updated 04 / 2026. Visit the official EUDAMED website for up-to-date data.

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Notified Bodies

BSI Group The Netherlands B.V. DEKRA Certification B.V. DNV Product Assurance AS POLSKIE CENTRUM BADAN I CERTYFIKACJI S.A. SGS Belgium NV TÜV Rheinland LGA Products GmbH TÜV SÜD Product Service GmbH UDEM Uluslararasi Belgelendirme Denetim Egitim Merkezi San. ve Tic. A.Ş.

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