18 results · 24ms · Sources: EU EUDAMED, US FDA

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Reprocessed Livewire Steerable Diagnostic Electrophysiology Catheter

FDA 510(k)
FDA Class 2 ·Cardiovascular

Bernafon

FDA UDI
Bernafon AG·05711584090336·ZERENA 3 MNR FW 3.0

Ophthalmic Retractor

FDA UDI
KATENA PRODUCTS, INC.·00841668101094·HELVESTON "BIG BARBIE" RETRACTOR 9MM

MClass

FDA UDI
Conmed Corporation·10845854021040·MCLASS OSCILLATING SAW BLADE 19 X 1.27 (0.050")...

CONMED

FDA UDI
Conmed Corporation·10845854021453·OSCILLATING SAW BLADE 19 X 1.27 X 90 MM

ConMed Linvatec

FDA UDI
Provision·B504OMT190127900·

CONMED

FDA UDI
Conmed Corporation·10845854021446·OSCILLATING SAW BLADE 19 X 1.27 X 105 MM

MClass

FDA UDI
Conmed Corporation·10845854021033·MCLASS OSCILLATING SAW BLADE 19 X 1.27 (0.050")...

VIDAS® GDH

FDA Adverse Event
Malfunction ·BIOMERIEUX SA·Product code MCB·May 25, 2018

VIDAS® C. DIFFICILE GDH

FDA Adverse Event
Malfunction ·BIOMERIEUX SA·Product code MCB·May 1, 2018

METATARSAL DECOMPRESSION IMPLANT, MODEL 100

FDA 510(k)
FDA Class 2 ·Orthopedic

ELI 230 ELECTROCARDIOGRAPH

FDA 510(k)
FDA Class 2 ·Cardiovascular

TENDRIL DX

FDA Adverse Event
Malfunction ·ST. JUDE MEDICAL, INC. CRMD·Product code DTB·January 11, 2014

STENOSCOP

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 18, 2013

INTERNAL PADDLES OPTION FOR DEFIBRILLATOR/MONITOR

FDA Adverse Event
Malfunction ·PHILIPS HEALTHCARE - ANDOVER·Product code MKJ·June 30, 2011

OT ULTRA2 METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·September 7, 2012

OSCILLATING SAW BLADE 19 X 1.27 X 105MM QTY 5

FDA Adverse Event
Injury ·CONMED LARGO·Product code GFA·April 5, 2023

Aquapak 340 SW, 340, mL w/040 Adaptor, Teleflex Medical, respiratory gas humidifier adaptor.

FDA Enforcement
Class II ·Terminated·Teleflex Medical·July 16, 2014