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EUDAMED
FDA 510(k)
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GUDID
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Manufacturer: Kelyniam Global Inc.
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Device
Device · Manufacturer · Authorizations
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Verified
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Status
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Regime
Registry
Registry
Class
Class
Kelyniam Csi Peek-IM1001
Kelyniam Global Inc.
·
,
FDA registration: United States
GUDID
not on market
Withdrawn
Registry:
GUDID
Class
Class:
II
Kelyniam Csi Peek-IM1004
Kelyniam Global Inc.
·
,
FDA registration: United States
GUDID
not on market
Withdrawn
Registry:
GUDID
Class
Class:
II
Kelyniam Csi Peek-IM1002
Kelyniam Global Inc.
·
,
FDA registration: United States
GUDID
not on market
Withdrawn
Registry:
GUDID
Class
Class:
II
Kelyniam Csi Peek-IM2003
Kelyniam Global Inc.
·
,
FDA registration: United States
GUDID
not on market
Withdrawn
Registry:
GUDID
Class
Class:
II
Kelyniam Csi Peek-IM1003
Kelyniam Global Inc.
·
,
FDA registration: United States
GUDID
not on market
Withdrawn
Registry:
GUDID
Class
Class:
II
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