28 results · 21ms · Sources: EU EUDAMED, US FDA

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U-RIGHT TD-4279 BLOOD GLUCOSE MONITORING SYSTEM, FORA GD40/TD-4272 BLOOD GLUCOSE MONITORING SYSTEM

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

Tasso+

FDA UDI
Tasso Inc.·00860006434595·

Hallux Osteotomy Plate

FDA UDI
I.T.S. GmbH·09120034308543·Hallux Osteotomy Plate, 9mm

GUTTA PERCHA POINTS

FDA UDI
DiaDent Group International·08806383501347·Gutta Percha Points is used to root canal filin...

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172973646·

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172973561·

STOCKERT V172 SERIES VENOUS FEMORAL CANNULAE

FDA 510(k)
FDA Class 2 ·Cardiovascular

BARRETT UNICONDYLAR TIBIAL BEARING

FDA 510(k)
FDA Class 2 ·Orthopedic

BD VACUTAINER® RAPID SERUM TUBE (RST) BLOOD COLLECTION TUBES THROMBIN

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code JKA·May 9, 2018

BD VACUTAINER® RAPID SERUM TUBE (RST) BLOOD COLLECTION TUBES THROMBIN

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code JKA·May 1, 2018

BD VACUTAINER® RAPID SERUM TUBE (RST) BLOOD COLLECTION TUBES THROMBIN

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code JKA·May 22, 2018

LUX 1440

FDA Adverse Event
Malfunction ·PALOMAR MEDICAL TECHNOLOGIES, INC.·Product code GEX·May 5, 2012

BD VACUTAINER® RAPID SERUM TUBE (RST) BLOOD COLLECTION TUBES THROMBIN

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code JKA·June 8, 2018

BD VACUTAINER® RAPID SERUM TUBE (RST) BLOOD COLLECTION TUBES THROMBIN

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code JKA·April 26, 2018

BD VACUTAINER® RAPID SERUM TUBE (RST) BLOOD COLLECTION TUBES THROMBIN

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code JKA·April 20, 2018

EQUINOXE

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code KWT·July 2, 2019

BD VACUTAINER® RAPID SERUM TUBE (RST) BLOOD COLLECTION TUBES THROMBIN

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code JKA·May 22, 2018

9800

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 2, 2013

ARCHITECT TOTAL T3

FDA Adverse Event
Malfunction ·A.I.D.D LONGFORD·Product code CDP·September 19, 2014

MILD DEVICE KIT

FDA Adverse Event
Injury ·VERTOS MEDICAL INC.·Product code HRX·May 18, 2011