61 results · 27ms · Sources: EU EUDAMED, 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