27 results
·
23ms
·
Sources: EU EUDAMED, US FDA
DIVER C.E. CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
KOMET Surgical Saw Blade
FDA UDI
Gebr. Brasseler GmbH & Co. KG·14053613049891·
KOMET Surgical Saw Blade
FDA UDI
Gebr. Brasseler GmbH & Co. KG·14053613070079·
KOMET Surgical Saw Blade
FDA UDI
Gebr. Brasseler GmbH & Co. KG·14053613274743·
KOMET Surgical Saw Blade
FDA UDI
Gebr. Brasseler GmbH & Co. KG·14053613274644·
KOMET Surgical Saw Blade
FDA UDI
Gebr. Brasseler GmbH & Co. KG·14053613274828·
KOMET Surgical Saw Blade
FDA UDI
Gebr. Brasseler GmbH & Co. KG·14053613064344·
KM Blade
FDA UDI
Gebr. Brasseler GmbH & Co. KG·14053613216965·Sawblade sterile for Stryker®
62 x 27,6 x 1,00/...
KOMET Surgical Saw Blade
FDA UDI
Gebr. Brasseler GmbH & Co. KG·14053613294383·
ADVANCED HIP ASSESSMENT SOFTWARE
FDA 510(k)
FDA Class 2
·Radiology
PARODI CATHETER FOR ANGIOGRAPHY (PARCA)
FDA 510(k)
FDA Class 2
·Cardiovascular
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 11, 2013
SKIN SHAVER PREP RAZOR STERILE
FDA Adverse Event
Malfunction
·TYCO HEALTHCARE/KENDALL·Product code LWK·May 23, 2008
VITALITY 2
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·April 12, 2011
BASEPLATE IMPACTOR, ASSEMBLY
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·May 29, 2024
BASEPLATE IMPACTOR, ASSEMBLY
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·June 5, 2024
UNIVERSAL GLENOID - CENTRAL SCREW 20MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code PHX·November 23, 2020
UNI GLENOID-PERIPHERAL LOCK SCRW
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code PHX·November 23, 2020
UNI GLENOID-PERIPHERAL LOCK SCRW
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code PHX·November 23, 2020
HUM INSERT L/42+3 TO FIT IN 42 CUP CONST
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code PHX·November 23, 2020