751 results
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24ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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AIRLIGHT DENTAL HANDPIECE
FDA 510(k)
FDA Class 1
·Dental
APEX®
FDA UDI
B. BRAUN MEDICAL INC.·04046955746781·SCB APEX 4000ML SINGLE PACK
n/a
FDA UDI
HANS RUDOLPH, INC.·00874750006595·1410BB 2WAY NRBV W/BODY SALIVA
REPROCESSED EXTERNAL FIXATION DEVICE
FDA 510(k)
FDA Class 2
·Orthopedic
BLUE POWDERFREE NITRILE EXAMINATION GLOVE
FDA 510(k)
FDA Class 1
·General Hospital
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
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
RESERVOIR 3ML
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·May 14, 2013
ULTRACISION HARMONIC SCALPEL CURVED SHEARS (LCS) - PISTOL GRIP 36 CM - 15 MM ACT
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC·Product code GEI·August 11, 2008
PINNACLE MULTIHOLE II CUP 66MM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code LPH·May 19, 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
BIPAP A40 PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·September 11, 2024
BIPAP A40 PRO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·September 11, 2024