43 results
·
25ms
·
Sources: EU EUDAMED, US FDA
800 SERIES EASYNEB NEBULIZER
FDA 510(k)
FDA Class 2
·Anesthesiology
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·H65820203571·Channels Glide Path File NiTi
Midway Select
FDA UDI
MIDWAY DENTAL SUPPLY, LLC·10843717103575·Midway Select Disposable Diamonds 379-023M Pkg/25
EZ CONNECT RESIN
FDA 510(k)
FDA Class 2
·Dental
100 S AND 100 LC AND 485 ANSER ULTRASOUND IMAGING SYSTEMS
FDA 510(k)
FDA Class 2
·Radiology
TRANSEND GUIDEWIRE
FDA Adverse Event
Malfunction
·NEUROVASCULAR DIVISION, BOSTON SCIENTIFIC CORP·Product code DQX·October 27, 2009
EECP THERAPY SYSTEM, MODEL TS3
FDA Adverse Event
Injury
·VASOMEDICAL, INC.·Product code DRN·December 30, 2002
TRANSEND GUIDEWIRE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 7, 2010
TRANSEND GUIDEWIRE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 10, 2010
TRANSEND GUIDEWIRE
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MIAMI·Product code DQX·July 14, 2010
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
TRANSEND GUIDEWIRE
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MIAMI·Product code DQX·November 9, 2010
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