61 results
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27ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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3D GraftRasp System
FDA 510(k)
FDA Class 2
·General Hospital
Dornier MedTech
FDA UDI
Dornier MedTech GmbH·04049958002625·Medilas HRM UroPulse Holmium Laser with wired f...
Blade Handle
FDA UDI
KATENA PRODUCTS, INC.·00841668112366·CHUCK HANDLE #3K 10CM LONG
Blade Handle
FDA UDI
KATENA PRODUCTS, INC.·00841668112373·CHUCK HANDLE #3KA 7.5CM LONG
Blade Handle
FDA UDI
KATENA PRODUCTS, INC.·00841668112380·BARD-PARKER HANDLE #3
PARADIGM REAL-TIME INSULIN INFUSION PUMP MMT-722RNAB
FDA Adverse Event
Death
·MEDTRONIC MINIMED·Product code OYC·February 11, 2020
iTotal Identity Posterior Stabilized Knee Replacement System
FDA UDI
Conformis, Inc.·M572RPS0201900031·ITOTAL IDENTITY PS TIBIAL INSERT + TRIAL, IPOLY...
iTotal Identity CR
FDA UDI
Conformis, Inc.·M572RCR0201900141·ITOTAL IDENTITY CR TIBIAL INSERT, NO TRIAL, IPO...
iTotal Identity CR
FDA UDI
Conformis, Inc.·M572RCR0201900041·ITOTAL IDENTITY CR TIBIAL INSERT + TRIAL, IPOLY...
iTotal PS
FDA UDI
Conformis, Inc.·M572RPS0201900121·ITOTAL PS IPOLY XE - 19MM INSERT - LEFT or righ...
ENZYME IMMUNOASSAY ANTI-SSDNA ANTIBODY TEST
FDA 510(k)
FDA Class 2
·Immunology
HAKKI URINARY CATHETER; SIZE 14, 16, 18, 20, 22, 24, 26 FRENCH
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
670G INSULIN PUMP MMT-1780KL
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·December 20, 2019
ARROW
FDA Adverse Event
Malfunction
·FH INDUSTRIE·Product code KWS·May 22, 2026
MICA SCREW
FDA Adverse Event
Injury
·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code HWC·October 8, 2019
MICA SCREW
FDA Adverse Event
Injury
·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code HWC·October 8, 2019
MICA SCREW
FDA Adverse Event
Injury
·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code HWC·October 8, 2019
MICA SCREW
FDA Adverse Event
Injury
·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code HWC·October 8, 2019
PUMP MMT-1780KPK 670G PATHWAY BLACK MG
FDA Adverse Event
Death
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·April 26, 2024
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·June 19, 2020