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Variants of Xpert® by CEPHEID
3 variants
Key
Device
Device · Manufacturer · Authorizations
Verified
Verified
Status
Status
Regime
Regime
Registry
Registry
Class
Class
Xpert®
UDI-DI 07332940006013
Cepheid
·
,
United States
FDA 510(k)
K151565
Active
Cleared 16 Oct 2015
CE/IVDR
Active
Regimes:
CE IVDR
510(k)
Registry:
EUDAMED
Class
Class:
A
Xpert®
UDI-DI 07332940002305
Cepheid
·
,
United States
CE/IVDR
Active
Regimes:
CE IVDR
Registry:
EUDAMED
Class
Class:
A
Xpert®
UDI-DI 07332940001865
Cepheid
·
,
United States
CE/IVDR
Active
Regimes:
CE IVDR
Registry:
EUDAMED
Class
Class:
A
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