10 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SAFETY INFUSION SET
FDA 510(k)
FDA Class 2
·General Hospital
Cutimed® Sorbion®
FDA UDI
BSN medical GmbH·04042809708417·CUTIMED SORBION CARBON PLUS STERILE 15X25CM 10
BIOMET MICROFIXATION STERNAL CLOSURE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
PROVEN MODULAR POSTERIOR STABILIZED FEMORAL
FDA 510(k)
FDA Class 2
·Orthopedic
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·May 21, 2013
ORTHOPAT PERIOPERATIVE AUTOTRANSFUSION SYSTEM
FDA Adverse Event
Malfunction
·HAEMONETICS CORP.·Product code CAC·May 23, 2011
HARMONIC ACE 23CM
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC·Product code LFL·August 13, 2008
INSPIRE 8F DUAL
FDA Adverse Event
Malfunction
·SORIN GROUP ITALIA·Product code DTN·January 9, 2026
BD SYRINGE CATHETER TIP 50ML
FDA Adverse Event
Malfunction
·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code KYZ·December 9, 2025
INSPIRE 6 HOLLOW FIBER OXYGENATOR W/ INTEGRATED HARDSHELL VENOUS/CARDIOTOMY RES
FDA Adverse Event
SORIN GROUP ITALIA S.R.L.·Product code DTZ·December 7, 2016