23 results · 22ms · Sources: EU EUDAMED, US FDA

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Dual Pump Pack

FDA 510(k)
FDA Class 2 ·Ophthalmic

MW-1000 IONTOPHORETIC DRUG DELIVERY ELECTRODE

FDA 510(k)
FDA Class 2 ·Physical Medicine

STAIR SYSTEMS PACS & DICOM VIEWER

FDA 510(k)
FDA Class 2 ·Radiology

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·May 3, 2023

MICRUSFRAME10 6MM X 11.9CM

FDA Adverse Event
Malfunction ·MEDOS INTERNATIONAL SARL·Product code KRD·July 8, 2022

16MM CANN PERCUTANEOUS HOLLOW DRILL BIT

FDA Adverse Event
Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code LXH·May 2, 2019

CARELINK

FDA Adverse Event
Malfunction ·MEDTRONIC INC.·Product code KRG·October 10, 2014

TENSION FREE VAGINAL TAPE

FDA Adverse Event
Injury ·ETHICON, INC.·Product code PAH·June 10, 2013

HOMECHOICE AUTOMATED PD SET WITH CASSETTE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·July 13, 2011

UNIVERSA FIRM URETERAL STENT SET

FDA Adverse Event
Malfunction ·COOK INC·Product code FAD·June 25, 2019

UNIVERSA FIRM URETERAL STENT SET

FDA Adverse Event
Malfunction ·COOK INC·Product code FAD·June 25, 2019

UNIVERSA FIRM URETERAL STENT SET

FDA Adverse Event
Malfunction ·COOK INC·Product code FAD·June 26, 2019

UNIVERSA FIRM URETERAL STENT SET

FDA Adverse Event
Malfunction ·COOK INC·Product code FAD·December 31, 2019

UNIVERSA FIRM URETERAL STENT SET

FDA Adverse Event
Malfunction ·COOK INC·Product code FAD·December 31, 2019

16MM CANNULATED HOLLOW DRILL BIT

FDA Adverse Event
Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code LXH·February 3, 2020

UNIVERSA FIRM URETERAL STENT SET

FDA Adverse Event
Injury ·COOK INC·Product code FAD·June 14, 2019

UNIVERSA FIRM URETERAL STENT SET

FDA Adverse Event
Malfunction ·COOK INC·Product code FAD·June 26, 2019

UNKNOWN

FDA Adverse Event
Malfunction ·COOK INC·Product code FAD·July 23, 2019

UNIVERSA FIRM URETERAL STENT SET

FDA Adverse Event
Malfunction ·COOK INC·Product code FAD·August 27, 2019

16MM CANNULATED HOLLOW DRILL BIT

FDA Adverse Event
Malfunction ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code LXH·May 16, 2018