23 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Portex NRFit Epidural Needles, Portex NRFit Spinal Needles, Portex NRFit Loss of Resistance (L.O.R.) Syringes., Portex EpiFuse Catheter Connector, Portex Regional Anaesthesia Portfolio Filters
FDA 510(k)
FDA Class 2
·Anesthesiology
BreastBoard SX™
FDA UDI
MACROMEDICS B.V.·08719425707174·BreastBoard SX baseplate, 2P, bottomstop and in...
OsteoMed
FDA UDI
OSTEOMED LLC·00845694027151·2.4mm X 10mm Cannulated Headless Screw
Ophthalmic Ring
FDA UDI
KATENA PRODUCTS, INC.·00841668100820·FLIERINGA FIXATION RING 21MM
G8 Curved Cup Inserter
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215057794·
OsteoMed
FDA UDI
OSTEOMED LLC·00845694068741·Cannulated 2.4 x 10mm Headless Screw Sterile Qty 5
KSEA CLEARVISION II, MODEL 40334120
FDA 510(k)
FDA Class 2
·Neurology
MATRYX INTERFERENCE SCREW (5.0-6.5MM)
FDA 510(k)
FDA Class 2
·Orthopedic
NUTRILINE
FDA Adverse Event
Malfunction
·VYGON USA·Product code LJS·May 2, 2023
PEN NDL 32G 4MM PRO 100 BOX 1200 CA
FDA Adverse Event
Malfunction
·EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND·Product code FMI·July 3, 2024
PEN NDL 32G 4MM PRO 100 BOX 1200 CA
FDA Adverse Event
Malfunction
·EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND·Product code FMI·July 3, 2024
PEN NDL 32G 4MM PRO 100 BOX 1200 CA
FDA Adverse Event
Malfunction
·EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND·Product code FMI·July 3, 2024
PEN NDL 32G 4MM PRO 100 BOX 1200 CA
FDA Adverse Event
Malfunction
·EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND·Product code FMI·July 3, 2024
PEN NDL 32G 4MM PRO 100 BOX 1200 CA
FDA Adverse Event
Malfunction
·EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND·Product code FMI·July 3, 2024
PEN NDL 32G 4MM PRO 100 BOX 1200 CA
FDA Adverse Event
Malfunction
·EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND·Product code FMI·July 3, 2024
ARCHITECT TOTAL T3
FDA Adverse Event
Malfunction
·A.I.D.D LONGFORD·Product code CDP·October 15, 2014
NDHP MACRO PPR T CON
FDA Adverse Event
Malfunction
·HOSPIRA LTD.·Product code FPA·June 5, 2013
ACCU-CHEK TENDERLINK INFUSION SET
FDA Adverse Event
Malfunction
·ROCHE INSULIN DELIVERY SYSTEMS, INC.·Product code FPA·June 17, 2011
NUTRILINE
FDA Adverse Event
Malfunction
·VYGON USA·Product code LJS·March 28, 2023
NUTRILINE
FDA Adverse Event
Malfunction
·VYGON USA·Product code LJS·February 13, 2023