748 results
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28ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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BD VERITOR(TM) SYSTEM FOR THE RAPID DETECTION OF RSV
FDA 510(k)
FDA Class 1
·Microbiology
KIT RSV 30 TEST HOSPITAL VERITOR
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·April 15, 2021
LARGE CANNULATED SCREWS
FDA UDI
Smith & Nephew, Inc.·03596010063885·6.5MM UNIVERSAL CANNULATED SCREW 65MM
Bone cutters
FDA UDI
DFS - DIAMON GmbH·04057176148391·DIADOSS cutter
ECAT VISION PET SCANNER, MODELS 3000 & 5000
FDA 510(k)
FDA Class 2
·Radiology
NOVA MAX PLUS GLOCOSE AND B-KETONE CONTROL SOLUTION-MID, HIGH
FDA 510(k)
FDA Class 1
·Clinical Chemistry
BIPAP A40 PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·September 12, 2024
BIPAP A40 PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·September 11, 2024
BONE SCREW Ø6,5 H.25MM
FDA Adverse Event
Malfunction
·LIMACORPORATE S.P.A.·Product code LPH·January 25, 2022
BIPAP A40
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·September 9, 2024
BIPAP A40 PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·September 6, 2024
BIPAP A40 PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·September 13, 2024
OPTISENSE
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code DTB·January 13, 2014
UNKNOWN DEPUY DEVICE
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JDI·May 21, 2013
DEPUY ASR FEM IMPLANT SZ 46
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KXA·June 2, 2011
BIPAP A40 PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·September 16, 2024
BIPAP A40 PRO, IT
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·September 5, 2025
BIPAP A40 PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·June 5, 2024
BIPAP A40 PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·June 6, 2024
BIPAP A40 PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·June 5, 2024