23 results · 20ms · Sources: EU EUDAMED, US FDA

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TANDEMHEART TRANSSEPTAL CANNULA SET-EF, MODEL 5140-6221

FDA 510(k)
FDA Class 2 ·Cardiovascular

SOLIDEA

FDA UDI
CALZIFICIO PINELLI SRL·08300496055051·SAVANNAH LACE 70 KNEE-HIGH, SIZE S, NERO, GRADU...

SOLIDEA

FDA UDI
CALZIFICIO PINELLI SRL·08300496055037·SAVANNAH LACE 70 KNEE-HIGH, SIZE M, MOKA, GRADU...

SOLIDEA

FDA UDI
CALZIFICIO PINELLI SRL·08300496055020·SAVANNAH LACE 70 KNEE-HIGH, SIZE S, MOKA, GRADU...

SOLIDEA

FDA UDI
CALZIFICIO PINELLI SRL·08300496055068·SAVANNAH LACE 70 KNEE-HIGH, SIZE M, NERO, GRADU...

SOLIDEA

FDA UDI
CALZIFICIO PINELLI SRL·08300496055105·SAVANNAH LACE 70 KNEE-HIGH, SIZE L, ANTRACITE, ...

SOLIDEA

FDA UDI
CALZIFICIO PINELLI SRL·08300496055082·SAVANNAH LACE 70 KNEE-HIGH, SIZE S, ANTRACITE, ...

SOLIDEA

FDA UDI
CALZIFICIO PINELLI SRL·08300496055044·SAVANNAH LACE 70 KNEE-HIGH, SIZE L, MOKA, GRADU...

SOLIDEA

FDA UDI
CALZIFICIO PINELLI SRL·08300496055075·SAVANNAH LACE 70 KNEE-HIGH, SIZE L, NERO, GRADU...

SOLIDEA

FDA UDI
CALZIFICIO PINELLI SRL·08300496055099·SAVANNAH LACE 70 KNEE-HIGH, SIZE M, ANTRACITE, ...

JACOBS HIGH VACUUM SUCTION UNIT 05-2570

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

MEDCOMP REPAIR KIT, MODEL ASPCRPK

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

BIO-LOGIC CEEGRAPH NETLINK

FDA 510(k)
FDA Class 2 ·Neurology

G2 FILTER SYSTEM

FDA Adverse Event
Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·August 21, 2007

G2 FILTER SYSTEM

FDA Adverse Event
Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·May 15, 2007

RECOVERY G2 FILTER SYSTEM - JUGULAR DELIVERY KIT

FDA Adverse Event
Injury ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·March 23, 2010

DELTA

FDA Adverse Event
Malfunction ·HISTORICAL CPI ST. PAUL·Product code NVZ·April 11, 2013

ACRYSOF

FDA Adverse Event
Injury ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·April 8, 2011

BRAVO

FDA Adverse Event
Malfunction ·ARIZONA DEVICE MANUFACTURING·Product code FFT·May 22, 2008

MEDTRONIC SURGICAL ANNULOPLASTY PRODUCTS

FDA Adverse Event
Injury ·MEDTRONIC HEART VALVES DIVISION·Product code KRH·October 26, 2021