23 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Grasping Forceps
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772814534·GENUMEDI SAND SIZE II
n.a.
FDA UDI
Karl Storz GmbH & Co. KG·04048551057650·Ear Loop, size 2, 16 cm
PILLING
FDA UDI
TELEFLEX INCORPORATED·24026704509021·
Custom Healthcare Systems Inc.
FDA UDI
Manus Medical, LLC·00811870033124·
Recon
FDA UDI
Revelation Medical Devices·G31810152802·Double B Retractor
MANAN BIO-CUT SOFT TISSUE BIOPSY NEEDLE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
INTEGRA ELECTRODE TUNNELING NEEDLE
FDA 510(k)
FDA Class 2
·Neurology
RESOLUTION 360 CLIP
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code PKL·December 2, 2024
Medline-Microtek
FDA UDI
Microtek Medical LLC·20748426262902·Set Up Cover, 112 cm x 178 cm (44 in x 70 in)
Medline-Microtek
FDA UDI
Microtek Medical LLC·20748426263558·Set Up Cover, 112 cm x 229 cm (44 in x 90 in)
Medline-Microtek
FDA UDI
Microtek Medical LLC·20748426262919·Set Up Cover with Label, 137 cm x 229 cm (54 in...
Medline-Microtek
FDA UDI
Microtek Medical LLC·20748426262315·Set Up Cover, 137 cm x 229 cm (54 in x 90 in)
WALLSTENT RP ENDOPROSTHESIS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code JCT·March 21, 2025
WALLSTENT ENDOPROSTHESIS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code MAF·December 22, 2025
WALLSTENT ENDOPROSTHESIS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code MAF·December 1, 2025
SYSTEM, PERITONEAL, AUTOMATIC DELIVERY
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FKX·October 8, 2014
PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE
FDA Adverse Event
Injury
·RICE CREEK MFG·Product code LWP·June 8, 2013
COLLEAGUE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 7, 2011
WALLSTENT? RP ENDOPROSTHESIS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FGE·July 21, 2025