17 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Libertas Acetabular Hooded Liner
FDA 510(k)
FDA Class 2
·Orthopedic
Padded Arm Sling
FDA UDI
MEDICAL SPECIALTIES INCORPORATED·00802357833658·
BOSS Instruments
FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515028661·Initial Incision Retractor, large blade, 1 x 1.5"
MobileLink Acetabular Cup System
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575177134·E-Dur Insert
MobileLink Acetabular Cup System
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575177141·E-Dur Insert
MobileLink Acetabular Cup System
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575177158·E-Dur Insert
INFANT ARRAY
FDA 510(k)
FDA Class 2
·Radiology
DISCOVERY 3T 16 CH BODY ARRAY COIL (ANTERIOR); DISCOVERY 3T 16 CH BODY ARRAY COIL (POSTERIOR); DISCOVERY 3T 32 CH BODY A
FDA 510(k)
FDA Class 2
·Radiology
EKOSONIC ENDOVASCULAR DEVICE, 135X12CM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KRA·February 3, 2023
EKOSONIC ENDOVASCULAR DEVICE, 135X12CM
FDA Adverse Event
Death
·BOSTON SCIENTIFIC CORPORATION·Product code KRA·February 3, 2023
EKOSONIC ENDOVASCULAR DEVICE, 106X12CM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KRA·March 1, 2023
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 18, 2014
ACCESS® ACCUTNI?
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code MMI·June 21, 2013
SOFTCLIX® LANCET DEVICE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code FMK·July 28, 2011
EKOSONIC ENDOVASCULAR DEVICE, 106X18CM
FDA Adverse Event
Death
·BOSTON SCIENTIFIC CORPORATION·Product code KRA·February 3, 2023
PHOTOFIX PATCH - 6CM X 8CM
FDA Adverse Event
Injury
·CRYOLIFE, INC. - KENNESAW·Product code PSQ·January 12, 2021
PEDICLE SCREW 03.50.054 PEDICLE SCREW 8X40MM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code NKB·June 16, 2023