49 results
·
21ms
·
Sources: EU EUDAMED, US FDA
GUARDIAN URETHRAL SHEATH
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Tyber Medical
FDA UDI
Tyber Medical, LLC·M695002C1412520·Cervical Curved 14 x 12 x 5 ° Trial
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973851·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970904·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970898·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973141·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973318·
ACUITY (TM) CUT-AWAY (TM) GUIDE CATHETERS 6F AND 8F
FDA 510(k)
FDA Class 2
·Cardiovascular
NEOTRACT ANCHOR SYSTEM MODEL: REF 11208
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973578·
980 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN·Product code CBK·December 14, 2016
PROPEX II EUR
FDA Adverse Event
Malfunction
·MAILLEFER INSTRUMENTS HOLDING SARL·Product code LQY·July 20, 2022
AUTOPULSE RESUSCITATION SYSTEM MODEL 100
FDA Adverse Event
Malfunction
·ZOLL CIRCULATION·Product code DRM·October 3, 2014
MERSILENE POLYESTER FIBER MESH
FDA Adverse Event
Injury
·ETHICON, INC.·Product code FTL·June 3, 2013
SOL 13.5 BOW RT 10.0 12/14
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code LPH·June 22, 2011
HF UNIT "ESG-400"
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code GEI·April 23, 2021
HF UNIT "ESG-400"
FDA Adverse Event
Injury
·OLYMPUS WINTER & IBE GMBH·Product code GEI·December 5, 2017
HF UNIT "ESG-400"
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code GEI·July 8, 2020
HF UNIT "ESG-400"
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code GEI·November 17, 2020
HF UNIT "ESG-400"
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code GEI·May 17, 2021