15 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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TE ME NA EPIDURAL CATHETER
FDA 510(k)
FDA Class 2
·Anesthesiology
Stryker CrossFlow Integrated Arthroscopy Pump
FDA 510(k)
FDA Class 2
·Orthopedic
ETHICON ENDO-SURGERY FLEXIBLE BIPOLAR HEMOSTASIS FORCEPS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ZEPHIR ANTERIOR CERVICAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDIC INC.·Product code KWQ·June 11, 2009
EXTENSION SET
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·March 6, 2013
X7000 XENON LIGHTSOURCE
FDA Adverse Event
Malfunction
·STRYKER ENDOSCOPY SAN JOSE·Product code FCW·January 25, 2011
CAPSUREFIX NOVUS
FDA Adverse Event
Malfunction
·MPRI·Product code DTB·August 8, 2014
DURAL ALPHA INSERT W RIM II/32
FDA Adverse Event
Malfunction
·ZIMMER GMBH·Product code LPH·March 12, 2019
DURASUL, ALPHA INSERT, HOODED, II/32
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code LPH·September 28, 2018
METASUL, ALPHA INSERT, JJ/28
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWA·February 4, 2019
DURASUL, ALPHA INSERT, KK/36
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code JDI·March 13, 2018
COCR HEAD 32/ 0 'M' 12/14
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code JDI·June 4, 2019
DURASUL, ALPHA INSERT, LL/36
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code JDI·April 29, 2019
L.C. 5000/CE 2-CHANNEL PUMP (50/CASE)
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FPA·August 22, 2013
DURASUL, ALPHA INSERT, HOODED, KK/32
FDA Adverse Event
Malfunction
·ZIMMER GMBH·Product code LPH·June 15, 2018