46 results
·
25ms
·
Sources: EU EUDAMED, US FDA
AUDIOSCREENER OAE
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
EQUATE
FDA UDI
WAL-MART STORES, INC.·00078742082868·THIN LINERS REGULAR UNSCENTED 120 CT
Indeflator
FDA UDI
ABBOTT VASCULAR INC.·08717648013591·20/30 INDEFLATOR Inflation Device 30 atm 20 cc
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·10304040054397·Polycarbonate Crowns
truFreeze
FDA UDI
US Endoscopy·00724995199333·Rapid AV Active Venting Cathether is used with ...
truFreeze
FDA UDI
Csa Medical, Inc.·10857068006102·Rapid AV Catheter, box of 5
truFreeze
FDA UDI
Csa Medical, Inc.·00857068006105·Rapid AV Catheter
AIM 100
FDA UDI
Burton Medical, LLC·00858480006049·FLOOR BASE ASSEMBLY
AIM 100
FDA UDI
Burton Medical, LLC·00858480006247·FLOOR BASE ASSEMBLY
RS-4M+MUSCLE STIMULATOR
FDA 510(k)
FDA Class 2
·Physical Medicine
ENRAF-NONIUS SONOPULS 190 SYSTEM
FDA 510(k)
FDA Class 2
·Physical Medicine
BALL HEADS: COCR BALL HEAD 12/14 36 SIZE M 0
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JDI·October 20, 2020
20/30 PRIORITY PACK INDEFLATOR
FDA Adverse Event
Malfunction
·ABBOTT VASCULAR·Product code MAV·July 20, 2021
GREENFIELD¿
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - CORK·Product code DTK·March 12, 2013
SM204 M-SERIES W/BIG WHEEL
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FPO·February 3, 2011
THIN WALLED GORE-TEX STRETCH VASCULAR GRAFT
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES, INC.·Product code DSY·February 19, 2008
20/30 PRIORITY PACK INDEFLATOR
FDA Adverse Event
Malfunction
·ABBOTT VASCULAR·Product code MAV·April 20, 2021
20/30 INDEFLATOR -REF 1000184 WPL2122268-01 (2019-03-01)
FDA Recall
Open, Classified
·Abbott Vascular·Product code MAV·March 11, 2022
PEARL EDGE BELL CUP
FDA Adverse Event
Injury
·COOPERSURGICAL, INC.·Product code HDB·August 22, 2024
20/30 PRIORITY PACK INDEFLATOR
FDA Adverse Event
Malfunction
·ABBOTT VASCULAR·Product code MAV·July 20, 2021