11 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MANAN EPIDURAL NEEDLE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704284232·
NAR
FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209110490·
Sklar®
FDA UDI
SKLAR CORPORATION·10649111192999·MCCREA XS URETHRAL SOUND 28FR
2.4MM SYSTEM
FDA UDI
BIOMET MICROFIXATION, INC·00841036083748·
SensiCare PI Surgical Gloves
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
RESOLUTION ENDOVASCULAR SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
TERUMO TCM II COLLING AND HEATING SYSTEM
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DWC·November 13, 2012
RESERVOIR 3ML
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·June 5, 2014
OCTRODE PERCUTANEOUS LEAD
FDA Adverse Event
Injury
·ADVANCED NEUROMODULATION SYSTEMS, INC.·Product code LGW·September 29, 2010
BARD Dynamic Deca Steerable, Product Number 201101; REPROCESSED ELECTROPHYSIOLOGY CATHETER
FDA Enforcement
Class II
·Ongoing·Stryker Sustainability Solutions·May 20, 2026