18 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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XIAN FRIENDSHIP DISPOSABLE NERVE STIMULATOR PROBES
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
P&P marker for SenoRX 10G
FDA UDI
Noras MRI products GmbH·04251269202247·
Probe
FDA UDI
ELLIQUENCE, LLC·00846338006839·
BD INSYTE AUTOGUARD PNK 20GA X 1.16IN
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·December 16, 2022
UniTip Catheter
FDA UDI
Unisensor AG·07640172971369·
Gibralt
FDA UDI
Choice Spine, LP·00840996169448·GIBRALT,DRILL,FIXED,2.4X26
UniTip Catheter
FDA UDI
Unisensor AG·07640172973233·
CARESCAPE MODEL V100 VITAL SIGNS MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
DYNA-EXTOR II
FDA 510(k)
FDA Class 2
·Orthopedic
BD BBL¿ TB AURAMINE M
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code KJK·April 16, 2026
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·May 14, 2013
12X100MM KII FIOS FIRST ENTRY THREADED 6/BOX
FDA Adverse Event
APPLIED MEDICAL·Product code GCJ·March 15, 2011
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·September 24, 2014
SCREWDRIVER BIT T15, AO FITTING
FDA Adverse Event
Malfunction
·STRYKER GMBH·Product code HWC·October 6, 2017
SCREWDRIVER BIT T15, AO FITTING
FDA Adverse Event
Malfunction
·STRYKER GMBH·Product code HWC·October 6, 2017
EMBLEM S-ICD Model A209
FDA Enforcement
Class I
·Terminated·Boston Scientific Corporation·February 17, 2021
INLIVEN CRT-P, Model Numbers: a) V284 b) V285 c) W274 d) W275 (added 7/15/2021)
FDA Enforcement
Class I
·Ongoing·Boston Scientific Corporation·July 21, 2021
Model Number L131, ESSENTIO DR EL MRI Pacemaker
FDA Enforcement
Class I
·Ongoing·Boston Scientific Corporation·October 22, 2025