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

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INFUSET FLOW CONTROL EXTENSION SET

FDA 510(k)
FDA Class 2 ·General Hospital

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·00636257125137·20-30 MV FOR MEN CLSC CALF STD TAN III

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·00636257127261·20-30 MV FOR MEN SEL CALF STD TAN III

N/A

FDA UDI
BIOMET MICROFIXATION, INC·00841036032029·

Millennium

FDA UDI
Avalign Technologies, Inc.·00190776127701·Holtz Suction Extraction Tip, Diameter 4.0mm OL...

Stage-1

FDA UDI
KEYSTONE DENTAL, INC.·D768S14013301K0·Drill

DANmed

FDA UDI
DANNORITZER Medizintechnik GmbH & Co. KG·04251351105036·LAP-Instrument, Ø5mm, l=330mm, detach. Graspi...

DANmed

FDA UDI
DANNORITZER Medizintechnik GmbH & Co. KG·04251351112812·LAP-Instrument, Ø5mm, l=330mm, detach. Graspi...

DANmed

FDA UDI
DANNORITZER Medizintechnik GmbH & Co. KG·04251351102875·LAP-Instrument, Ø5mm, l=330mm, flushp. Graspi...

DANmed

FDA UDI
DANNORITZER Medizintechnik GmbH & Co. KG·04251351109089·LAP-Instrument, Ø5mm, l=330mm, flushp. Graspi...

DANmed

FDA UDI
DANNORITZER Medizintechnik GmbH & Co. KG·04251351110948·LAP-Instrument, Ø5mm, l=330mm, detach. Graspi...

DANmed

FDA UDI
DANNORITZER Medizintechnik GmbH & Co. KG·04251351115417·LAP-Instrument, Ø5mm, l=330mm, detach. Graspi...

DANmed

FDA UDI
DANNORITZER Medizintechnik GmbH & Co. KG·04251351117718·LAP-Insert only, Ø5mm, l=330mm Graspi...

AIRSTRIP REMOTE PATIENT MONITORING (RPM) REMOTE DATA VIEWING SOFTWARE, VERSION 3.1

FDA 510(k)
FDA Class 2 ·Cardiovascular

URINE AMPHETAMINE/METHAMPHETAMINE SCREEN FLEX REAGENT CARTRIDGE

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

VIDAS HCG

FDA Adverse Event
Malfunction ·BIOMERIEUX SA·Product code JLW·November 26, 2020

ROD, UNKNOWN SIZE

FDA Adverse Event
Injury ·ZIMMER BIOMET SPINE INC.·Product code MNH·May 14, 2019

5.5 TI CANNULATED TRANSLATION SCREW, UNKNOWN SIZE

FDA Adverse Event
Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·November 27, 2019

PROMUS PREMIER?

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·October 3, 2014

SHILEY XLT

FDA Adverse Event
Malfunction ·COVIDIEN·Product code JOH·May 29, 2013