23 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BD PROBETEC CHLAMYDIA TRACHOMATIS (CT) QX AMPLIFIED DNA ASSAY
FDA 510(k)
FDA Class 1
·Microbiology
Orthopedic manual surgical instrument
FDA UDI
BAUI BIOTECH CO. LTD.·04715862873575·Poly Axial Screw Driver
LEONE SPA
FDA UDI
LEONE SPA·08033707065708·INTRAORAL ELASTICS 4,5 oz 1/4" red
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450047903·
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197513548·RZ Tebbet Breast Retractor
90x24m...
PERSONAL INFUSOR LOCAL PAIN MANAGEMENT PROCEDURAL KIT
FDA 510(k)
FDA Class 2
·General Hospital
PERCUTANEOUS INTRODUCER, MODEL 10383-XXX
FDA 510(k)
FDA Class 2
·Cardiovascular
TGS UKA SYSTEM
FDA Adverse Event
Injury
·ALEXANDRIA RESEARCH TECHNOLOGIES, INC·Product code HSX·March 22, 2013
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·April 17, 2025
TGS UKA KNEE SYSTEM
FDA Adverse Event
Injury
·ALEXANDRIA RESEARCH TECHNOLOGIES, INC.·Product code HSX·May 6, 2013
ADULT DUAL HEATED BREATHING CIRCUIT
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE, LTD.·Product code BZE·December 8, 2009
TGS UKA SYSTEM
FDA Adverse Event
Injury
·CAYENNE MEDICAL, INC·Product code HSX·February 12, 2014
TGS UKA SYSTEM
FDA Adverse Event
Injury
·CAYENNE MEDICAL, INC.·Product code HSX·September 25, 2014
UNKNOWN GEL IMPLANTS
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code FTR·December 27, 2019
UNKNOWN GEL IMPLANTS
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code FTR·December 27, 2019
TGS UKA SYSTEM
FDA Adverse Event
Injury
·CAYENNE MEDICAL INC.·Product code HSX·May 15, 2014
TGS UKA KNEE SYSTEM
FDA Adverse Event
Injury
·ALEXANDRIA RESEARCH TECHNOLOGIES, INC.·Product code HSX·September 10, 2013
TGS UKA KNEE SYSTEM
FDA Adverse Event
Injury
·ALEXANDRIA RESEARCH TECHNOLOGIES, LLC·Product code HSX·August 14, 2013
XIENCE XPEDITION EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code NIQ·May 2, 2013
TERUMO ADVANCED PERFUSION SYSTEM 1
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTQ·April 26, 2011