37 results · 31ms · Sources: EU EUDAMED, US FDA

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SYNTHETIC ABSORBABLE SUTURE

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

OsteoMed

FDA UDI
OSTEOMED LLC·00845694045919·PrimaLIF LLIF PEEK Implant, 7mm X 22mm X 35mm, ...

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197527590·Titanium Gerald Forceps, straight diamon...

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197415286·Titanium Gerald Forceps, straight diamon...

POWDER FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)

FDA 510(k)
FDA Class 1 ·General Hospital

MODIFIED VERTE-STACK SPINAL SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

3.5FR URETHANE UMB CATH

FDA Adverse Event
Malfunction ·COVIDIEN MANUFACTURING SOLUTIONS SA·Product code FOS·September 9, 2014

1.9F ARGYLE SINGLE LUMEN PICC

FDA Adverse Event
Malfunction ·COVIDIEN·Product code LJS·September 18, 2014

3.5FR P.U.R. UMBIL CATH X10

FDA Adverse Event
Malfunction ·COVIDIEN·Product code FOS·June 3, 2014

2.5FR URETHANE UMB CATH

FDA Adverse Event
Malfunction ·COVIDIEN·Product code FOS·May 29, 2014

3.5FR URETHANE UMBCATH

FDA Adverse Event
Malfunction ·COVIDIEN·Product code FOS·June 17, 2014

2.5FR URETHANE UMB CATH

FDA Adverse Event
Malfunction ·COVIDIEN·Product code FOS·May 29, 2014

3.5FR P.U.R. UMBIL CATH X10

FDA Adverse Event
Malfunction ·COVIDIEN·Product code FOS·November 7, 2014

3.5FR P.U.R. UMBIL CATH X10

FDA Adverse Event
Malfunction ·COVIDIEN·Product code FOS·October 3, 2014

3.5 FR URETHANE UMB CATH

FDA Adverse Event
Malfunction ·COVIDIEN·Product code FOS·July 28, 2014

DUAL LUMEN INSERTION TRAY

FDA Adverse Event
Malfunction ·COVIDIEN, COVIDIEN MANUFACTURING·Product code LJS·September 18, 2014

DUAL LUMEN INSERTION TRAY

FDA Adverse Event
Malfunction ·COVIDIEN, COVIDIEN MANUFACTURING·Product code LJS·September 18, 2014

3.5FR URETHANE UMB CATH

FDA Adverse Event
Malfunction ·COVIDIEN·Product code FOS·August 22, 2014

3.5FR URETHANE UMB CATH

FDA Adverse Event
Malfunction ·COVIDIEN·Product code FOS·October 20, 2014

3.5FR DUAL-LUMEN UVC CATH

FDA Adverse Event
Malfunction ·COVIDIEN·Product code FOS·October 20, 2014