14 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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ATTEST Drug Screen Cup, ATTEST Drug Screen Dip Card
FDA 510(k)
FDA Class 2
·Clinical Toxicology
7450 RV2 MASK
FDA UDI
HANS RUDOLPH, INC.·00874750002726·HEADGEAR LARGE V2MASK REUSEBL
SPECIAL, EMPOWR ACETABULAR, CANNULATED CUP IMPACTOR
FDA Adverse Event
Malfunction
·ENCORE MEDICAL L.P·Product code LXH·June 26, 2023
ABSORBENT PAPER POINTS
FDA UDI
DiaDent Group International·08806383511858·"An absorbent paper points is an endodontic pap...
GDC POWER SUPPLY
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - FREMONT·Product code HCG·July 20, 2010
GDC POWER SUPPLY, MODEL GDC POWER SUPPLY: 451007-4
FDA 510(k)
FDA Class 2
·Neurology
MODIFICATION TO PROMPT L-POP
FDA 510(k)
FDA Class 2
·Dental
ACCU-CHEK ® AVIVA PLUS TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·July 28, 2014
SHILEY PERCUTANEOUS
FDA Adverse Event
Injury
·COVDIEN/FORMERLY TYCO HE·Product code BTO·October 17, 2008
EON 16-CHANNEL IPG
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·August 4, 2011
LUMAX 740 VR-T DX PROMRI
FDA Adverse Event
Malfunction
·BIOTRONIK SE & CO. KG·Product code LWS·July 2, 2013
ZENITH FLEX WITH SPIRAL-Z TECHNOLOGY AAA ENDOVASCULAR GRAFT ILIAC LEG
FDA Adverse Event
Injury
·COOK INC·Product code MIH·December 19, 2017
ZENITH FLEX WITH SPIRAL-Z TECHNOLOGY AAA ENDOVASCULAR GRAFT ILIAC LEG
FDA Adverse Event
Injury
·COOK INC·Product code MIH·December 19, 2017
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