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Results for “DeepRESP”
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EUDAMED
1
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Iceland
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4 devices found
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Device · Manufacturer · Authorizations
Verified
Status
Regime
Registry
Class
DeepRESP
Nox Medical Ehf
Class II
FDA 510(k)
K241960
Active
Cleared 14 Mar 2025
Active
510(k)
510(k)
II
2 variants
DeepRESP
K252330
DeepRESP
Nox Medical Ehf
Class II
GUDID
on market
None
GUDID
II
DeepRESP
Nox Medical
·
,
Iceland
Class IIa
CE/MDR
Active
CE MDR
EUDAMED
IIa
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