29 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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TOP DRAPE STERILE, TOP DRAPE-NON STERILE, BOTTOM DRAPE- STERILE, BOTTOM DRAPE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Color Cuff
FDA UDI
STRYKER CORPORATION·07613154599585·Disposable Tourniquet Cuff Single Bladder, Sing...
Surgical Instrument
FDA UDI
Jeil Medical Corporation·08806390880787·
Surgical Instrument
FDA UDI
Jeil Medical Corporation·08806390880794·
Stryker
FDA UDI
Provision·B504TQ59211121360·
Surgical Instrument
FDA UDI
Jeil Medical Corporation·08806390880770·
Summa Orthopaedics System Surgical Instrument
FDA UDI
Jeil Medical Corporation·08800089402847·
VESSEL GUARDIAN
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
AVITA AGIL IT 101 INSTANT DIGITAL THERMOMETER
FDA 510(k)
FDA Class 2
·General Hospital
Tandry Locking Plate System
FDA UDI
MICROWARE PRECISION CO., LTD.·04719873106202·3.5mm Locking Distal Fibula Plate, 3 Holes, Right
Summa Orthopaedics System Surgical Instrument
FDA UDI
Jeil Medical Corporation·08800089402861·
Summa Orthopaedics System Surgical Instrument
FDA UDI
Jeil Medical Corporation·08800089402878·
Summa Orthopaedics System Surgical Instrument
FDA UDI
Jeil Medical Corporation·08800089402854·
LIFEVEST WCD 4000 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL LIFECOR CORPORATION·Product code MVK·May 3, 2013
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 2, 2011
LIFEPAK CR PLUS DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC.·Product code MKJ·August 6, 2008
INTROCAN SAFETY® 3
FDA Adverse Event
Malfunction
·B BRAUN MELSUNGEN AG·Product code FOZ·November 14, 2025
INTROCAN SAFETY® 3
FDA Adverse Event
Malfunction
·B BRAUN MELSUNGEN AG·Product code FOZ·November 12, 2025
INTROCAN SAFETY® 3
FDA Adverse Event
Malfunction
·B BRAUN MELSUNGEN AG·Product code FOZ·February 20, 2026
INTROCAN SAFETY® 3
FDA Adverse Event
Injury
·B BRAUN MELSUNGEN AG·Product code FOZ·October 6, 2025