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