11 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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SUPRA 577.Y LASER
FDA 510(k)
FDA Class 2
·Ophthalmic
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450535912·
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450210352·
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450276884·
AMERITEK BRACHYTHERAPY TEMPLATE
FDA 510(k)
FDA Class 2
·Radiology
LACTOSORB 5.0 MM WASHER
FDA 510(k)
FDA Class 2
·Orthopedic
DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·April 18, 2024
CURRENT PLUS DR
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL INC., CRMD·Product code LWS·January 13, 2014
2.5MM DHS/DCS GUIDE WIRE W/THREADED TIP 230MM
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code HWC·May 3, 2013
5F POLYURETHANE UMBILICAL CATHETER
FDA Adverse Event
Injury
·VYGON SA·Product code FOS·April 27, 2011
Stryker MA204 Bed Model (FL25E) Beds are intended for medical purposes in both general patient care as well as critical care environments. Each uses built-in electric motors and controls which can be operated by the patient, or caregiver, to adjust the height and/or surface contour of the bed.The devices listed above also include movable and latchable side rails which can be lowered or raised to help prevent patient fall and subsequent injury. The Beds include an optional Scale (Models: FL20E, FL25E, FL28C, FL28EX) as well as an optional Bed Exit (1 Zone) or Chaperone
FDA Enforcement
Class II
·Terminated·Stryker Medical Division of Stryker Corporation·July 4, 2012