11 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BACTIDROP(TM) DOBELL & O'CONNOR IODINE
FDA 510(k)
FDA Class 1
·Microbiology
NA
FDA UDI
Stryker Leibinger GmbH & Co. KG·07613154185474·FULL SIZE LID UNIVERSAL II
Novo Surgical
FDA UDI
NOVO SURGICAL, INC.·G5869130060·osteotome caps, gas or steam permeable, latex-f...
WARMTOUCH COMPACT WARMING UNIT
FDA Adverse Event
Malfunction
·COVIDIEN/FORMERLY TYCO·Product code DWJ·December 23, 2010
I-FUSE HAMMER TOE SYSTEMS
FDA 510(k)
FDA Class 2
·Orthopedic
OVUS CAPLESS SAFETY NEEDLE
FDA 510(k)
FDA Class 2
·General Hospital
WARM TOUCH II COMPACT WARMING UNIT
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY TYCO HEALTHCARE·Product code DWJ·September 24, 2010
PRIMARY TRITANIUM HEMI CLUSTER HOLE CUP 52MM
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·January 14, 2013
LIFEVEST WCD 4000 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL LIFECOR CORPORATION·Product code MVK·November 18, 2010
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORP.·Product code FRN·January 14, 2014
Alcon Custom Pak
FDA Enforcement
Class II
·Ongoing·Alcon Research, LTD.·August 23, 2023