36 results
·
25ms
·
Sources: EU EUDAMED, US FDA
TOSCA 500 PCO2, SPO2 AND PULSE RATE MONITORING SYSTEM, MODEL 5202009
FDA 510(k)
FDA Class 2
·Anesthesiology
ACQSIM-MULTISLICE-CT, MODEL 453567042271
FDA 510(k)
FDA Class 2
·Radiology
ARCPM 1050 RESIN-HIPS
FDA 510(k)
FDA Class 2
·Orthopedic
RINGLOC-X ARCOMXL H/W 50/32MM 23
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code LPH·May 10, 2016
RINGLOC-X ARCOMXL H/W 54/36MM 24
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code LPH·July 1, 2016
RINGLOC-X ARCOM LINER
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·July 20, 2017
RINGLOC-X E1 H/W 60/36MM 26
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·July 20, 2016
RINGLOC-X E1 H/+3MM 50/36MM 23
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·February 1, 2016
ARCOM XL HI-WALL LINER RINGLOC-X SZ 46MM (RINGLOC SIZE 22)
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code LPH·July 29, 2016
RINGLOC-X E1 H/W 60/36MM 26
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·July 20, 2016
ARCOM XL HI-WALL LINER RINGLOC-X SZ 54MM (RINGLOC SIZE 24)
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code LPH·April 20, 2016
ARCOM XL HI-WALL LINER RINGLOC-X SZ 46MM (RINGLOC SIZE 22)
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code LPH·July 29, 2016
ARCPM 1050 RESIN-HIPS
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code LPH·April 5, 2017
E1 10DEG LINER RINGLOC-X 58MM
FDA Adverse Event
Malfunction
·.·Product code LPH·May 11, 2017
RLOC-X E1 H/W +3MM 50/36MM 23
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code LPH·August 26, 2019
PRECISION®
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·April 9, 2013
TYSHAK II CATHETER
FDA Adverse Event
Malfunction
·NUMED, INC.·Product code DQY·February 25, 2011
ENDOTAK ENDURANCE EZ
FDA Adverse Event
Injury
·CARDIAC PACEMAKERS, INC·Product code LWS·May 8, 2008
E1 HI-WALL LINER RINGLOC-X 60/36MM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·March 7, 2017
RINGLOC-X E1 H/W 58/40MM 25
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code LPH·July 6, 2016