23 results · 25ms · Sources: EU EUDAMED, 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