66 results
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26ms
·
Sources: EU EUDAMED, US FDA
ABCO MIDSTREAM URINE COLLECTION SET
FDA 510(k)
FDA Class 1
·Pathology
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772777655·LUMBAMED BASIC DORSAL STAYS M SILVER III
PLIER
FDA UDI
Ortho Arch Company Inc·D90980023313·RAZOR LOOP FORMING PLIER
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197418799·Malleable Retractor Blade
76x152...
MENICON SF-P
FDA 510(k)
FDA Class 2
·Ophthalmic
SUDOSCAN
FDA 510(k)
FDA Class 2
·Neurology
NOVASURE IMPEDANCE CONTROLLED EA SYSTEM
FDA Adverse Event
Injury
·HOLOGIC·Product code MNB·April 30, 2014
GOBED II MED/SURG BED
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·October 8, 2012
FREESTYLE FLASH
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC, USA·Product code LFR·August 31, 2007
S-SPOT REF 777, 777S Adhere to skin for marking and identifying moles in mammography.
FDA Recall
Terminated
·Beekley Corporation·Product code JAC·June 13, 2018
O-SPOT REF 791, 791S Adhere to skin for marking and identifying moles in mammography.
FDA Recall
Terminated
·Beekley Corporation·Product code JAC·June 13, 2018
TomoSPOT REF 782, 782S, 783, 783S, 784, 784S, 785 & 785S Adhere to skin for marking and identifying moles in mammography.
FDA Recall
Terminated
·Beekley Corporation·Product code JAC·June 13, 2018
ECMO Reinforced Dual Lumen Cannula, 28Fr., REF: VV28F, Sterile EO Indications: The OriGen Reinforced Dual Lumen Cannula is indicated for use as a single cannula for both venous drainage and re-infusion of blood in the internal jugular vein during extracorporeal life support procedures.
FDA Recall
Terminated
·OriGen Biomedical, Inc.·Product code DWF·August 21, 2018
Reinforced Dual Lumen Cannula, 19Fr., REF: VV19F, Sterile EO Indications: The OriGen Reinforced Dual Lumen Cannula is indicated for use as a single cannula for both venous drainage and re-infusion of blood in the internal jugular vein during extracorporeal life support procedures.
FDA Recall
Terminated
·OriGen Biomedical, Inc.·Product code DWF·August 21, 2018
Reinforced Dual Lumen Cannula, 23Fr., REF: VV23F, Sterile EO Indications: The OriGen Reinforced Dual Lumen Cannula is indicated for use as a single cannula for both venous drainage and re-infusion of blood in the internal jugular vein during extracorporeal life support procedures.
FDA Recall
Terminated
·OriGen Biomedical, Inc.·Product code DWF·August 21, 2018
Reinforced Dual Lumen Cannula, 32Fr., REF: VV32F, Sterile EO Indications: The OriGen Reinforced Dual Lumen Cannula is indicated for use as a single cannula for both venous drainage and re-infusion of blood in the internal jugular vein during extracorporeal life support procedures.
FDA Recall
Terminated
·OriGen Biomedical, Inc.·Product code DWF·August 21, 2018
Reinforced Dual Lumen Cannula, 13Fr., REF: VV13F, Sterile EO; and ECMO Reinforced Dual Lumen Cannula, 13Fr., REF: VV13F, Sterile EO Indications: The OriGen Reinforced Dual Lumen Cannula is indicated for use as a single cannula for both venous drainage and re-infusion of blood in the internal jugular vein during extracorporeal life support procedures.
FDA Recall
Terminated
·OriGen Biomedical, Inc.·Product code DWF·August 21, 2018
Reinforced Dual Lumen Cannula, 16Fr., REF: VV16F, Sterile EO Indications: The OriGen Reinforced Dual Lumen Cannula is indicated for use as a single cannula for both venous drainage and re-infusion of blood in the internal jugular vein during extracorporeal life support procedures.
FDA Recall
Terminated
·OriGen Biomedical, Inc.·Product code DWF·August 21, 2018
Beekley Medical 0-SPOT Mammography Skin Markers REF 652
FDA Recall
Terminated
·Beekley Corporation·Product code JAC·May 8, 2017
Bella Blanket Protective Coverlet, for Mammography, 18cm x 25cm or 24cm x 30cm, Product Code: 311. The purpose of the product is to remove the cold by placing this sheet between the patients breast and the imaging receptor plate.
FDA Recall
Terminated
·Beekley Corporation·Product code IZH·July 2, 2012