29 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LTV 1000 VENTILATOR
FDA 510(k)
FDA Class 2
·Anesthesiology
N/A
FDA UDI
GEORGE TIEMANN & CO.·B58210517670·
ASSUFIL
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
DIAMEDIX IS-CMV IGM CAPTURE TEST SYSTEM
FDA 510(k)
FDA Class 2
·Microbiology
PORTABLE AIR COMPRESSOR FOR MEDICAL PURPOSES
FDA Adverse Event
MEDEL S.P.A.·Product code BTI·April 10, 2013
JAGWIRE GUIDEWIRE
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code DQX·May 21, 2008
ENDOTAK SQ
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code LWS·April 12, 2011
CRANI PACK, Model/Catalog Number WECR41D, medical procedure kit.
FDA Enforcement
Class II
·Ongoing·American Contract Systems Inc·March 26, 2025
UNIVERSA SILICONE FOLEY CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code EZL·September 25, 2018
UNIVERSA SILICONE FOLEY CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code EZL·September 26, 2018
UPJ OCCLUSION BALLOON CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code EZN·April 7, 2017
UNIVERSA SILICONE FOLEY CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code EZL·July 8, 2019
UNIVERSA SILICONE FOLEY CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code EZL·November 14, 2017
UNIVERSA SILICONE FOLEY CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code EZL·November 19, 2018
UNIVERSA SILICONE FOLEY CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code EZL·July 19, 2018
UNIVERSA SILICONE FOLEY CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code EZL·August 1, 2018
UNIVERSA SILICONE FOLEY CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code EZL·August 22, 2018
UNIVERSA SILICONE FOLEY CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code EZL·February 21, 2018
UNIVERSA SILICONE FOLEY CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code EZL·January 25, 2018
UNIVERSA SILICONE FOLEY CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code EZL·May 14, 2018