43 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Xingyu Nitrile Powder Free Patient Examination Gloves, White color
FDA 510(k)
FDA Class 1
·General Hospital
NA
FDA UDI
KEY SURGICAL, INC.·10849771049859·Steinmann Pins, Double diamond, .1563 inch (4.0...
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704293685·
DD tempMED
FDA UDI
Dental Direkt GmbH·EDDIK116151·DD tempMED are pre-colored dental milling blank...
FIXAFLOSS
FDA 510(k)
FDA Class 1
·Dental
POWERWIRE RADIOFREQUENCY GUIDEWIRE
FDA 510(k)
FDA Class 2
·Cardiovascular
OVUM ASPIRATION NEEDLE SINGLE LUMEN
FDA Adverse Event
Injury
·WILLIAM A. COOK AUSTRALIA, PTY LTD·Product code MQE·April 19, 2018
OVUM ASPIRATION NEEDLE SINGLE LUMEN
FDA Adverse Event
Injury
·WILLIAM A. COOK AUSTRALIA, PTY LTD·Product code MQE·April 22, 2018
COLON DECOMPRESSION SET
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FEG·November 8, 2022
OVUM ASPIRATION NEEDLE SINGLE LUMEN
FDA Adverse Event
Injury
·WILLIAM A. COOK AUSTRALIA, PTY LTD·Product code MQE·April 18, 2018
COLON DECOMPRESSION SET
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FEG·November 8, 2022
COLON DECOMPRESSION SET
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FEG·November 8, 2022
COLON DECOMPRESSION SET
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FEG·November 8, 2022
COLON DECOMPRESSION SET
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FEG·November 7, 2022
COLON DECOMPRESSION SET
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FEG·November 8, 2022
OVUM ASPIRATION NEEDLE SINGLE LUMEN
FDA Adverse Event
Injury
·WILLIAM A. COOK AUSTRALIA, PTY LTD·Product code MQE·April 19, 2018
OVUM ASPIRATION NEEDLE SINGLE LUMEN
FDA Adverse Event
Injury
·WILLIAM A. COOK AUSTRALIA, PTY LTD·Product code MQE·April 22, 2018
COLON DECOMPRESSION SET
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FEG·February 15, 2022
COLON DECOMPRESSION SET
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FEG·November 10, 2022
VITALITY
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 21, 2011